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Authors
Brabin, Bernard
Tinto, Halidou
Roberts, Stephen A.
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Clinical Trials BETA
Clinical trials referenced in this document:
nct01210040 at ClinicalTrials.govDocuments that mention this clinical trial
Excess risk of preterm birth with periconceptional iron supplementation in a malaria endemic area: analysis of secondary data on birth outcomes in a double blind randomized controlled safety trial in Burkina Faso
https://doi.org/10.1186/s12936-019-2797-8
Testing an infection model to explain excess risk of preterm birth with long-term iron supplementation in a malaria endemic area
https://doi.org/10.1186/s12936-019-3013-6
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Funding
Funding for this research was provided by:
National Institutes of Health (U01HD061234-01A1)
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Article History
Received: 23 September 2019
Accepted: 16 November 2019
First Online: 26 November 2019
Ethics approval and consent to participate
: The clinical protocol was approved by the Liverpool School of Tropical Medicine, UK, Research Ethics Committee (LSTM/REC Research Protocol 10.55. Dec 2010); the Institutional Review Board of the Institute of Tropical Medicine, Antwerp, Belgium (IRB/AB/AC/016. February 2011); the Antwerp University Hospital Ethics Committee (EC/UZA. February 2011); in Burkina Faso the Institutional Ethics Committee of Centre Muraz (Comité d’Ethique Institutionnel du Centre Muraz, and the National Ethics Committee (Comité Ethique pour la Recherche en Santé, CERS. Ref 015-2010/CE-CM. January 2011). All participants provided informed consent in line with the Declaration of Helsinki, and consent procedures have been previously detailed [].
: All participants gave consent for publication of research findings.
: The authors declare that they have no competing interests.
