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Signed or thumb-printed informed consent was obtained from each mother prior to study participation.
Inclusion criteria were as follows: ≤20 wk gestation confirmed by ultrasound, residence in the defined catchment area, availability during the period of the study, and signed or thumb-printed informed consent.
Each participant in the study provided a signed/thumb-printed informed consent.
All ILI cases (patients and HCWs) received printed information and signed an informed consent form.
The printed form of this informed consent is sent to our laboratory.
Informed consent (printed in local language) was obtained from each patient and the Ethics Committee of the Centre approved this study.
A binder with detailed study information, including informed consent and print-based aids for telephone assessments, was sent to each person who met initial screening criteria.
After providing extensive printed and oral information, a hand-signed informed consent form will be attained by a clinical research physician.
Informed consent statement was printed on the form.
Informed consent statement was printed on the study form.
To satisfy the need of the health workers who spoke native languages, the CRFs and the informed consent forms were translated and printed in different languages.
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