Protocol Section
The Protocol Section is one of the main sections in ClinicalTrials.gov data structure. It contains protocol-related information for clinical trials, including identification, status, design, eligibility, and other key details about how the trial is structured and conducted.
Protocol Section path is as follows:
Study -> Protocol Section -> Protocol Modules (Identification, Status, Design, Eligibility, etc.)
Protocol Section
Ignite Creation Date:
2025-12-24 @ 11:04 PM
Ignite Modification Date:
2025-12-24 @ 11:04 PM
NCT ID:
NCT05730569
Description:
All the data collected during the DenBalo study will be pseudonymised (i.e., identifable data can still be linked to patient files by means of a code) and the key to the codes will only be accessible to the principal investigators, or his/her representative.
The collected pseudonymised data as well as the collected biological samples can be shared with other (future) researchers for future research projects and studies, exclusively in the context of the same disease/pathology or similar (i.e., in the interest of research on maternal, newborn and child health). This will be done within a strictly legal framework and in compliance with international laws on the protection of personal data.
Only anonymized data will be used in any type of documentation, reports or publications (in the medical scientific literature and/or at medical conferences).
Personal patient data will be stored for at least 25 years after the end of the study.
Study:
NCT05730569
Study Brief:
Description and Comparison of Biological Vulnerability in Small Vulnerable Newborns Versus Healthy Community Controls in Urban Burkina Faso