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Hospital staff trained in the study protocols explained the study and obtained consent before collection of data, and collected blood samples from mothers at time of delivery.
All volunteers were familiarized with the study equipment and tests before collection of data.
Informed consent was administered at birth and again at follow-up, before collection of data.
Written consent from participants as well as their guardians was obtained before collection of data.
All participants signed an informed consent form witnessed by the local health office before collection of data and blood samples.
All human subjects in the study were asked for their consent before collection of data, and all had complete rights to withdraw from the study at any time without any threat or disadvantage.
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To address this we will monitor attrition rates in the first 6 months of T2 data collection, as collection of T2 data will begin 12 months before collection of T1 data is complete.
Informed consent is obtained before collection of any data.
Informed consent was obtained from all study participants before collection of epidemiologic data through personal interview.
Before collection of CD data, proteins were buffer-exchanged into CD-appropriate buffer (50 mM Tris/H2SO4, pH 7.5, 200 mM K2SO4 and 1 mM DTT).
A reconnaissance survey was done before actual collection of data to have an overview of the study area and to determine the sample size.
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