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:
2025-12-26 @ 1:18 PM
Ignite Modification Date:
2025-12-26 @ 1:18 PM
NCT ID:
NCT02223806
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years
* Be in labor with an expected vaginal delivery, as assessed by the midwives
* Gestation age ≥ 37 weeks
* Received antenatal instructions on postnatal uterine tonus assessment
* Provided informed consent.
Exclusion Criteria:
* Age \<18
* Elective caesarean delivery
* Severe anemia (\<8g/dL)
* Placenta praevia
* Anticipated breech delivery
* Referred patients who have not received antenatal care (ANC) uterine tonus assessment instructions
* Multiple Pregnancy
* Intra uterine fetal death
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02223806
Study Brief:
Protocol Section:
NCT02223806