Clinical and phytochemical studies of Plantago major in pressure ulcer treatment: A randomized controlled trial.
Folk medicine
HPLC
Plantago major
Pressure ulcer
Quercetin
Stroke
Journal
Complementary therapies in clinical practice
ISSN: 1873-6947
Titre abrégé: Complement Ther Clin Pract
Pays: England
ID NLM: 101225531
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
received:
12
09
2020
revised:
05
01
2021
accepted:
25
01
2021
pubmed:
7
2
2021
medline:
5
5
2021
entrez:
6
2
2021
Statut:
ppublish
Résumé
Plantago major L. is used by local people to improve various wounds and lesions such as pressure ulcer. In this study, the therapeutic effects of P. major topical formulation on the stage 1 pressure ulcer in patients have been investigated. This randomized triple blind clinical trial study was performed on 130 patients. During the 14 days of study, each of the test and control groups was checked according to check list. Also the topical formulation was standardized by HPLC based on the amount of quercetin. The findings of this study indicated a significant difference in resolution of the damage between the test and control groups. Topical formulation was standardized by HPLC based on the quercetin (1.88 mg/100g) and no side effects associated with this topical formulation was found. The results confirmed the traditional use of P. major in resolution of the damage. CLINICAL TRIAL ID: (IRCT201609209014N117).
Sections du résumé
BACKGROUND
BACKGROUND
Plantago major L. is used by local people to improve various wounds and lesions such as pressure ulcer. In this study, the therapeutic effects of P. major topical formulation on the stage 1 pressure ulcer in patients have been investigated.
MATERIALS AND METHODS
METHODS
This randomized triple blind clinical trial study was performed on 130 patients. During the 14 days of study, each of the test and control groups was checked according to check list. Also the topical formulation was standardized by HPLC based on the amount of quercetin.
RESULTS
RESULTS
The findings of this study indicated a significant difference in resolution of the damage between the test and control groups. Topical formulation was standardized by HPLC based on the quercetin (1.88 mg/100g) and no side effects associated with this topical formulation was found.
CONCLUSION
CONCLUSIONS
The results confirmed the traditional use of P. major in resolution of the damage. CLINICAL TRIAL ID: (IRCT201609209014N117).
Identifiants
pubmed: 33548748
pii: S1744-3881(21)00024-4
doi: 10.1016/j.ctcp.2021.101325
pii:
doi:
Substances chimiques
Phytochemicals
0
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Pagination
101325Informations de copyright
Copyright © 2021. Published by Elsevier Ltd.