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:
2025-12-24 @ 2:28 PM
Ignite Modification Date:
2025-12-24 @ 2:28 PM
NCT ID:
NCT01373359
Eligibility Criteria:
Inclusion Criteria:
* Women with a gestational age \>28weeks
* singleton pregnancy with cephalic presentation anticipating a normal spontaneous vaginal delivery (including episiotomy)
* a haemoglobin ≥ 8g/dl upon presentation who were admitted to labour room in the KLE teaching hospital attached to J N Medical College, Belgaum
Exclusion Criteria:
* Women with pregnancy induced hypertension
* antepartum haemorrhage
* previous caesarean section or presence of uterine scar
* diagnosed chorioamnionitis
* oxytocin induction or augmentation of labour
* intrauterine death
* diagnosed medical disorders (such as diabetes, cardiac, renal and hepatic diseases, etc.) or those in active labour (defined as \>4 cm dilatation)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT01373359
Study Brief:
Protocol Section:
NCT01373359