Impact of the COVID-19 pandemic on a clinical trial of pneumococcal vaccine scheduling (PVS) in rural Gambia.
COVID-19
Clinical trial
Immunisation
Pandemic
Pneumococcal vaccine
Journal
Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253
Informations de publication
Date de publication:
14 Apr 2023
14 Apr 2023
Historique:
received:
02
11
2022
accepted:
30
03
2023
medline:
17
4
2023
entrez:
13
4
2023
pubmed:
14
4
2023
Statut:
epublish
Résumé
The COVID-19 pandemic represents an unprecedented challenge for clinical research. The Pneumococcal Vaccine Schedules (PVS) study is a non-inferiority, interventional trial in which infants resident in 68 geographic clusters are randomised to two different schedules for pneumococcal vaccination. From September 2019 onwards, all infants resident in the study area became eligible for trial enrolment at all Expanded Programme on Immunisation (EPI) clinics in the study area. Surveillance for clinical endpoints is conducted at all 11 health facilities in the study area. PVS is conducted as a collaboration between the Medical Research Council Unit The Gambia (MRCG) at LSHTM and the Gambian Ministry of Health (MoH). The COVID-19 pandemic caused many disruptions to PVS. MRCG instructed interventional studies that participant enrolment be suspended on 26 March 2020, and a public health emergency was declared in The Gambia on 28 March 2020. Enrolment in PVS restarted on 1 July 2020 and was suspended again on 5 August 2020 after The Gambia experienced a sharp increase in COVID-19 cases in late July 2020 and restarted again on 1 September 2020. During periods of suspended enrolment of infants at EPI clinics, PVS continued safety surveillance at health facilities, albeit with disruptions. During the periods of suspended enrolment, infants who had been enrolled before 26 March 2020 continued to receive the PCV schedule to which they had been randomly allocated based on their village of residence, whereas all other infants received the standard PCV schedule. Throughout 2020 and 2021, the trial faced numerous technical and operational challenges: disruption to MoH delivery of EPI services and clinical care at health facilities; episodes of staff illness and isolation; disruption of MRCG transport, procurement, communications and human resource management; and also a range of ethical, regulatory, sponsorship, trial monitoring and financial challenges. In April 2021, a formal review concluded that the pandemic had not compromised the scientific validity of PVS and that the trial should continue as per protocol. The continuing challenges that COVID-19 poses to PVS, and other clinical trials will persist for some time.
Identifiants
pubmed: 37055788
doi: 10.1186/s13063-023-07298-w
pii: 10.1186/s13063-023-07298-w
pmc: PMC10101732
doi:
Substances chimiques
Pneumococcal Vaccines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
271Informations de copyright
© 2023. The Author(s).
Références
Trials. 2022 Jan 24;23(1):71
pubmed: 35073989
J Med Ethics. 2000 Feb;26(1):37-43
pubmed: 10701170
BMJ Glob Health. 2022 Feb;7(2):
pubmed: 35190459
Arch Med Res. 2020 Oct;51(7):731-732
pubmed: 32522362
Am J Trop Med Hyg. 2020 Jun;102(6):1164-1165
pubmed: 32333545
Vaccine. 2022 Oct 19;40(44):6367-6373
pubmed: 36180374
Trials. 2022 Dec 28;23(1):1058
pubmed: 36578030
Trials. 2022 Jan 15;23(1):39
pubmed: 35033180