Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:55 AM
Ignite Modification Date:
2025-12-25 @ 3:55 AM
NCT ID:
NCT01108302
Eligibility Criteria:
Inclusion Criteria:
* gestational age \>=28 wks at enrollment
* anticipate spontaneous vaginal delivery
* hemoglobin \>=8 gm/dl
* delivery at home, sub-center, or primary health center
* delivery attended by Auxilliary Nurse Midwife
Exclusion Criteria:
* previous caesarean-section
* scheduled for caesarean-section
* antepartum bleeding during current pregnancy
* blood pressure \>140mm of Hg systolic and \>90mm of Hg diastolic
* in active labor at time of recruitment
* high risk medical conditions (diabetes, cardiac ailments, seizures, placenta previa, anticipated breech delivery
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT01108302
Study Brief:
Protocol Section:
NCT01108302