Moser, Wendelin
Batil, Annour Adoum
Ott, Rebekka
Abderamane, Moussa
Clements, Ruth
Wampfler, Rahel
Poppert, Sven
Steinmann, Peter
Allan, Fiona
Greter, Helena https://orcid.org/0000-0003-1844-3961
Funding for this research was provided by:
Rudolf Geigy Foundation
Article History
Received: 25 October 2021
Accepted: 21 December 2021
First Online: 7 January 2022
Declarations
:
: The study received approval from the ethics committee Northwest and Central Switzerland (reference no. BASEC Nr Req-2018-0120) and the ‘Comité National de Bioéthique du Tchad’ (CNBT) in N’Djamena, Chad (reference no. 134/PR/MESRI/SG/CNBT/2018). Research authorization was granted by the Chadian Ministry of Health and its ‘Direction de la Lutte contre la Maladie et de la Promotion de la Santé’ (reference no. 007/PR/MSP/DG/DLMPS/2018). Upon arrival in the study villages, an assembly was organized with the community representatives to discuss the study objectives and procedures. The traditional leaders, together with the local authorities, discussed the study and decided about concrete participation. Once a collective decision had been reached, written informed consent was obtained from the community representatives. In line with high illiteracy rates among the general population, individual participants consented orally. These consent procedures had received approval by the respective ethics committees. Those participants with a positive test result from either filtration or POC-CCA testing were invited to the health centre/health post and were administered praziquantel in the adequate dose (40 mg/kg) by the study nurse.
: All authors approved submission for publication of this manuscript.
: The authors declare that they have no competing interests.