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 @ 12:15 PM
Ignite Modification Date:
2025-12-24 @ 12:15 PM
NCT ID:
NCT05079061
Eligibility Criteria:
Inclusion Criteria:
* All women age ≥ 18 years (age of legal consent)
* Singleton pregnancy \>= 34 weeks
Exclusion Criteria:
* Women planning for Caesarean section
* Women with known risk factors for PPH, including grand multiparity (\>=4), multiple pregnancy, fibroid with size \>4cm, history of PPH, placenta previa, large-for-gestational age fetus (defined as EFW \>90th centile), polyhydramnios, and previous Caesarean section.
* Women with bleeding tendency or thrombocytopenia \< 100 x 109/L
* Women on anticoagulant or aspirin
* Women in whom use of misoprostol / syntocinon / syntometrine is contraindicated
* Women with known hypersensitivity to misoprostol / syntocinon / syntometrine
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05079061
Study Brief:
Protocol Section:
NCT05079061