questionsmedicales.fr
Disciplines des sciences naturelles
Science
Recherche
Recherche biomédicale
Expérimentation humaine
Expérimentation humaine : Questions médicales fréquentes
Termes MeSH sélectionnés :
{
"@context": "https://schema.org",
"@graph": [
{
"@type": "MedicalWebPage",
"name": "Expérimentation humaine : Questions médicales les plus fréquentes",
"headline": "Expérimentation humaine : Comprendre les symptômes, diagnostics et traitements",
"description": "Guide complet et accessible sur les Expérimentation humaine : explications, diagnostics, traitements et prévention. Information médicale validée destinée aux patients.",
"datePublished": "2024-01-06",
"dateModified": "2025-03-31",
"inLanguage": "fr",
"medicalAudience": [
{
"@type": "MedicalAudience",
"name": "Grand public",
"audienceType": "Patient",
"healthCondition": {
"@type": "MedicalCondition",
"name": "Expérimentation humaine"
},
"suggestedMinAge": 18,
"suggestedGender": "unisex"
},
{
"@type": "MedicalAudience",
"name": "Médecins",
"audienceType": "Physician",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "France"
}
},
{
"@type": "MedicalAudience",
"name": "Chercheurs",
"audienceType": "Researcher",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "International"
}
}
],
"reviewedBy": {
"@type": "Person",
"name": "Dr Olivier Menir",
"jobTitle": "Expert en Médecine",
"description": "Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale",
"url": "/static/pages/docteur-olivier-menir.html",
"alumniOf": {
"@type": "EducationalOrganization",
"name": "Université Paris Descartes"
}
},
"isPartOf": {
"@type": "MedicalWebPage",
"name": "Recherche biomédicale",
"url": "https://questionsmedicales.fr/mesh/D035843",
"about": {
"@type": "MedicalCondition",
"name": "Recherche biomédicale",
"code": {
"@type": "MedicalCode",
"code": "D035843",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "H01.770.644.145"
}
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Expérimentation sur soi-même",
"alternateName": "Autoexperimentation",
"url": "https://questionsmedicales.fr/mesh/D032762",
"about": {
"@type": "MedicalCondition",
"name": "Expérimentation sur soi-même",
"code": {
"@type": "MedicalCode",
"code": "D032762",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "H01.770.644.145.365.100"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Expérimentation humaine non thérapeutique",
"alternateName": "Nontherapeutic Human Experimentation",
"url": "https://questionsmedicales.fr/mesh/D033281",
"about": {
"@type": "MedicalCondition",
"name": "Expérimentation humaine non thérapeutique",
"code": {
"@type": "MedicalCode",
"code": "D033281",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "H01.770.644.145.365.750"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Expérimentation thérapeutique humaine",
"alternateName": "Therapeutic Human Experimentation",
"url": "https://questionsmedicales.fr/mesh/D036302",
"about": {
"@type": "MedicalCondition",
"name": "Expérimentation thérapeutique humaine",
"code": {
"@type": "MedicalCode",
"code": "D036302",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "H01.770.644.145.365.875"
}
}
}
],
"about": {
"@type": "MedicalCondition",
"name": "Expérimentation humaine",
"alternateName": "Human Experimentation",
"code": {
"@type": "MedicalCode",
"code": "D006805",
"codingSystem": "MeSH"
}
},
"author": [
{
"@type": "Person",
"name": "Peter Pickkers",
"url": "https://questionsmedicales.fr/author/Peter%20Pickkers",
"affiliation": {
"@type": "Organization",
"name": "Dept. of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, the Netherlands; Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: peter.pickkers@radboudumc.nl."
}
},
{
"@type": "Person",
"name": "Paul R Chapman",
"url": "https://questionsmedicales.fr/author/Paul%20R%20Chapman",
"affiliation": {
"@type": "Organization",
"name": "Clinical Tropical Medicine, QIMR Berghofer Medical Research Institute, Herston, Australia."
}
},
{
"@type": "Person",
"name": "Paul Giacomin",
"url": "https://questionsmedicales.fr/author/Paul%20Giacomin",
"affiliation": {
"@type": "Organization",
"name": "Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia."
}
},
{
"@type": "Person",
"name": "Alex Loukas",
"url": "https://questionsmedicales.fr/author/Alex%20Loukas",
"affiliation": {
"@type": "Organization",
"name": "Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia."
}
},
{
"@type": "Person",
"name": "James S McCarthy",
"url": "https://questionsmedicales.fr/author/James%20S%20McCarthy",
"affiliation": {
"@type": "Organization",
"name": "Clinical Tropical Medicine, QIMR Berghofer Medical Research Institute, Herston, Australia."
}
}
],
"citation": [
{
"@type": "ScholarlyArticle",
"name": "Spatial analysis of photoplethysmography in cutaneous squamous cell carcinoma.",
"datePublished": "2022-05-05",
"url": "https://questionsmedicales.fr/article/35513459",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1038/s41598-022-10924-3"
}
},
{
"@type": "ScholarlyArticle",
"name": "Healthcare accessibility in preconflict Syria: a comparative spatial analysis.",
"datePublished": "2022-05-04",
"url": "https://questionsmedicales.fr/article/35508340",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1136/bmjopen-2021-059210"
}
},
{
"@type": "ScholarlyArticle",
"name": "Spatial variations and determinants of optimal antenatal care service utilisation in Ethiopia: spatial and survey regression analysis.",
"datePublished": "2023-05-23",
"url": "https://questionsmedicales.fr/article/37229944",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1016/j.puhe.2023.04.010"
}
},
{
"@type": "ScholarlyArticle",
"name": "The underlying drivers of energy efficiency: a spatial econometric analysis.",
"datePublished": "2022-09-19",
"url": "https://questionsmedicales.fr/article/36117222",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1007/s11356-022-23037-1"
}
},
{
"@type": "ScholarlyArticle",
"name": "Spatial analysis of American cutaneous leishmaniasis in the state of Amazonas.",
"datePublished": "2024-04-19",
"url": "https://questionsmedicales.fr/article/38656046",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.11606/s1518-8787.2024058005662"
}
}
],
"breadcrumb": {
"@type": "BreadcrumbList",
"itemListElement": [
{
"@type": "ListItem",
"position": 1,
"name": "questionsmedicales.fr",
"item": "https://questionsmedicales.fr"
},
{
"@type": "ListItem",
"position": 2,
"name": "Disciplines des sciences naturelles",
"item": "https://questionsmedicales.fr/mesh/D010811"
},
{
"@type": "ListItem",
"position": 3,
"name": "Science",
"item": "https://questionsmedicales.fr/mesh/D012586"
},
{
"@type": "ListItem",
"position": 4,
"name": "Recherche",
"item": "https://questionsmedicales.fr/mesh/D012106"
},
{
"@type": "ListItem",
"position": 5,
"name": "Recherche biomédicale",
"item": "https://questionsmedicales.fr/mesh/D035843"
},
{
"@type": "ListItem",
"position": 6,
"name": "Expérimentation humaine",
"item": "https://questionsmedicales.fr/mesh/D006805"
}
]
}
},
{
"@type": "MedicalWebPage",
"name": "Article complet : Expérimentation humaine - Questions et réponses",
"headline": "Questions et réponses médicales fréquentes sur Expérimentation humaine",
"description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.",
"datePublished": "2025-05-03",
"inLanguage": "fr",
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Diagnostic",
"headline": "Diagnostic sur Expérimentation humaine",
"description": "Comment évaluer la sécurité d'un essai clinique ?\nQuels tests sont utilisés pour les essais cliniques ?\nComment identifier les effets secondaires ?\nQu'est-ce qu'un groupe témoin ?\nComment sont définis les critères d'inclusion ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-diagnostic"
},
{
"@type": "MedicalWebPage",
"name": "Symptômes",
"headline": "Symptômes sur Expérimentation humaine",
"description": "Quels symptômes surveiller lors d'un essai ?\nComment signaler un effet indésirable ?\nLes symptômes peuvent-ils varier selon les groupes ?\nQuels sont les symptômes courants des essais ?\nComment évaluer l'impact des symptômes ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-symptômes"
},
{
"@type": "MedicalWebPage",
"name": "Prévention",
"headline": "Prévention sur Expérimentation humaine",
"description": "Comment prévenir les effets indésirables ?\nQuelles sont les mesures de sécurité en essais ?\nComment informer les participants des risques ?\nQuelles sont les recommandations pour les participants ?\nComment évaluer la prévention dans les essais ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-prévention"
},
{
"@type": "MedicalWebPage",
"name": "Traitements",
"headline": "Traitements sur Expérimentation humaine",
"description": "Quels types de traitements sont testés ?\nComment sont administrés les traitements ?\nQu'est-ce qu'un traitement de contrôle ?\nComment évaluer l'efficacité d'un traitement ?\nLes traitements sont-ils personnalisés ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-traitements"
},
{
"@type": "MedicalWebPage",
"name": "Complications",
"headline": "Complications sur Expérimentation humaine",
"description": "Quelles complications peuvent survenir ?\nComment gérer les complications pendant un essai ?\nLes complications sont-elles documentées ?\nComment prévenir les complications graves ?\nQuelles sont les conséquences des complications ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-complications"
},
{
"@type": "MedicalWebPage",
"name": "Facteurs de risque",
"headline": "Facteurs de risque sur Expérimentation humaine",
"description": "Quels sont les facteurs de risque pour les essais ?\nComment évaluer les facteurs de risque ?\nLes facteurs de risque varient-ils selon les traitements ?\nComment minimiser les facteurs de risque ?\nLes facteurs de risque sont-ils communiqués aux participants ?",
"url": "https://questionsmedicales.fr/mesh/D006805?mesh_terms=Spatial+Analysis&page=2#section-facteurs de risque"
}
]
},
{
"@type": "FAQPage",
"mainEntity": [
{
"@type": "Question",
"name": "Comment évaluer la sécurité d'un essai clinique ?",
"position": 1,
"acceptedAnswer": {
"@type": "Answer",
"text": "La sécurité est évaluée par des comités d'éthique et des protocoles rigoureux."
}
},
{
"@type": "Question",
"name": "Quels tests sont utilisés pour les essais cliniques ?",
"position": 2,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des tests cliniques, biologiques et d'imagerie sont utilisés pour évaluer les effets."
}
},
{
"@type": "Question",
"name": "Comment identifier les effets secondaires ?",
"position": 3,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les effets secondaires sont identifiés par la surveillance des participants et des rapports."
}
},
{
"@type": "Question",
"name": "Qu'est-ce qu'un groupe témoin ?",
"position": 4,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un groupe témoin est un groupe de participants qui ne reçoit pas le traitement testé."
}
},
{
"@type": "Question",
"name": "Comment sont définis les critères d'inclusion ?",
"position": 5,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les critères d'inclusion sont définis par des caractéristiques spécifiques des participants."
}
},
{
"@type": "Question",
"name": "Quels symptômes surveiller lors d'un essai ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes à surveiller incluent la douleur, la fatigue et les réactions allergiques."
}
},
{
"@type": "Question",
"name": "Comment signaler un effet indésirable ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les participants doivent signaler tout effet indésirable à l'équipe de recherche immédiatement."
}
},
{
"@type": "Question",
"name": "Les symptômes peuvent-ils varier selon les groupes ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les symptômes peuvent varier selon le groupe de traitement et les caractéristiques des participants."
}
},
{
"@type": "Question",
"name": "Quels sont les symptômes courants des essais ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes courants incluent des nausées, des maux de tête et des réactions cutanées."
}
},
{
"@type": "Question",
"name": "Comment évaluer l'impact des symptômes ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'impact est évalué par des questionnaires et des échelles de mesure standardisées."
}
},
{
"@type": "Question",
"name": "Comment prévenir les effets indésirables ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "La prévention inclut une sélection rigoureuse des participants et une surveillance étroite."
}
},
{
"@type": "Question",
"name": "Quelles sont les mesures de sécurité en essais ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les mesures incluent des consentements éclairés, des évaluations de risques et des protocoles stricts."
}
},
{
"@type": "Question",
"name": "Comment informer les participants des risques ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les participants reçoivent des informations détaillées lors du processus de consentement éclairé."
}
},
{
"@type": "Question",
"name": "Quelles sont les recommandations pour les participants ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les participants doivent suivre les instructions de l'étude et signaler tout problème de santé."
}
},
{
"@type": "Question",
"name": "Comment évaluer la prévention dans les essais ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'évaluation se fait par des études de suivi et des analyses des données de sécurité."
}
},
{
"@type": "Question",
"name": "Quels types de traitements sont testés ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les traitements peuvent inclure des médicaments, des thérapies physiques ou des interventions chirurgicales."
}
},
{
"@type": "Question",
"name": "Comment sont administrés les traitements ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les traitements peuvent être administrés par voie orale, intraveineuse ou topique selon l'étude."
}
},
{
"@type": "Question",
"name": "Qu'est-ce qu'un traitement de contrôle ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un traitement de contrôle est un traitement standard utilisé pour comparer l'efficacité."
}
},
{
"@type": "Question",
"name": "Comment évaluer l'efficacité d'un traitement ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'efficacité est évaluée par des mesures cliniques et des résultats rapportés par les patients."
}
},
{
"@type": "Question",
"name": "Les traitements sont-ils personnalisés ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certains essais cliniques testent des traitements personnalisés basés sur le profil génétique."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications peuvent inclure des infections, des réactions allergiques ou des effets graves."
}
},
{
"@type": "Question",
"name": "Comment gérer les complications pendant un essai ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications sont gérées par des protocoles d'urgence et des soins médicaux appropriés."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles documentées ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, toutes les complications doivent être documentées dans les rapports d'étude."
}
},
{
"@type": "Question",
"name": "Comment prévenir les complications graves ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "La prévention passe par une évaluation rigoureuse des participants et un suivi constant."
}
},
{
"@type": "Question",
"name": "Quelles sont les conséquences des complications ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les conséquences peuvent inclure l'arrêt de l'essai, des soins médicaux supplémentaires ou des poursuites."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque pour les essais ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs de risque incluent l'âge, les antécédents médicaux et les comorbidités."
}
},
{
"@type": "Question",
"name": "Comment évaluer les facteurs de risque ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs de risque sont évalués par des questionnaires et des examens médicaux."
}
},
{
"@type": "Question",
"name": "Les facteurs de risque varient-ils selon les traitements ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les facteurs de risque peuvent varier selon le type de traitement et la population étudiée."
}
},
{
"@type": "Question",
"name": "Comment minimiser les facteurs de risque ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "La minimisation passe par une sélection rigoureuse des participants et des protocoles adaptés."
}
},
{
"@type": "Question",
"name": "Les facteurs de risque sont-ils communiqués aux participants ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les participants sont informés des facteurs de risque lors du consentement éclairé."
}
}
]
}
]
}
The primary treatment of the common malignancy squamous cell carcinoma is surgical removal. In this process, sufficient tissue removal is balanced against unnecessary mutilation. We recently presented...
There is scarce information about the allocation of health resources in Syria. Pre-existing inequalities were further intensified after the 2011 conflict which displaced over 50% of the population. Th...
We compared two methods to quantify the inpatient bed access: provider to population ratio (PPR) and two-step floating catchment area (2SFCA) method. We compared PPR calculated at the governorate leve...
We found high inequality in access to public hospitals across and within governorates, especially in the north and eastern regions, where all governorates ranked in the lowest two quintiles using both...
Methodologically, the use of 2SFCA provided more nuanced insights about hospital bed allocation than PPR. 2SFCA was able to account for the cross-boundary effect and road network quality. Realistic re...
Optimal antenatal care (ANC) services are the main strategy to reduce maternal and newborn mortality. Understanding the geographic variation of ANC service utilisation is essential for regional- and l...
This was a spatial and survey regression analysis....
The secondary analysis of the Ethiopian Demographic and Health Survey 2019 was performed to investigate the spatial variation and determinants of optimal ANC service utilisation among women who were p...
Of 3979 pregnant women, 1656 (41.62%) had optimal ANC visits in Ethiopia. Optimal ANC utilisation was shown more prevalent in Northern, Eastern, Central and Northwestern regions of Ethiopia. The resul...
Optimal ANC service utilisation showed significant spatial dependency in Ethiopia, with spatial clustering in the Northern and Northwestern regions of the country. In addition, the results from this s...
It is theoretical and practical to investigate the causes and effects of energy efficiency. However, few empirical studies have been conducted to examine the potential underlying drivers of energy eff...
To evaluate, using spatial analysis, the occurrence of American Cutaneous Leishmaniasis (ACL) and analyze its association with the municipal human development index (MHDI) and deforestation in the sta...
This ecological study, carried out from January 2016 to December 2020, included the 62 municipalities of the state of Amazonas. The incidence rate of ACL was determined in space and time. Using Multip...
A total of 7,499 cases of ACL were registered in all 62 municipalities in the state. Most cases were in male (n=5,924; 79.24%), with the greatest frequency in the population aged from 20 to 39 years (...
The occurrence of ACL was evident in a variety of patterns in the state of Amazonas; the high incidence rates and persistence of this disease in this state were linked to deforestation. The temporal d...
Cooking and heating using solid fuels, such as dung, wood, agricultural residues, grass, straw, charcoal, and coal, is a main source of household air pollution. This indoor combustion encompasses a di...
The ability of fair investments in local general higher education to drive sustainable regional economic growth is explored. Based on spatial theory, the exploratory spatial data analysis method is us...
Syphilis remains a growing and resurging infectious disease in China. However, exploring the influence of environmental factors on the spatiotemporal distribution of syphilis remains under explore. Th...
The umbilical cord (UC) serves as the main pathway for bacteria to reach the neonate's body, potentially causing local and severe infections, sepsis, and even death. Consequently, neonatal mortality r...
A secondary data analysis of the Ethiopian Demographic Health Survey (EDHS 2016) was conducted using a weighted sample of 7,168 live births. ArcGIS version 10.7.1 software was utilized to visualize th...
Overall, the prevalence of harmful UCS care in Ethiopia was 15.09% (95% CI: 13.9-16.3), with significant spatial heterogeneity across geographical areas. The hotspot areas of harmful US care were obse...
In Ethiopia, the distribution of harmful UCS care practices is non-random and highly clustered in the SNNPR, Somalia, Tigray, and Amhara regions. Both individual and community-level factors were signi...
Low birth weight (LBW) is an important indicator of newborn health and can have long-term implications for a child's development. Spatial exploratory analysis provides a toolkit to gain insight into i...
We used data from the 2017 Ghana Maternal Health Survey and conducted individual-level and cluster-level analyses of LBW with place and zone of residence in both bivariate and multivariate analyses. B...
Ghana....
A total of 4127 women aged between 15 and 49 years were included in the individual-level analysis and 864 clusters corresponding to birth weight....
Individual and cluster-level distribution for LBW using spatial components for common determinants....
In the individual-level analysis, place and zone of residence were significantly associated with LBW in the bivariate model but not in a multivariate model. Hotspot analysis indicated the presence of ...
Our findings from choropleth hotspot maps suggest LBW clusters in Ghana's northern and middle zones. Disparities between the rural and urban continuum require specific attention to bridge the healthca...