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 @ 7:24 PM
Ignite Modification Date:
2025-12-24 @ 7:24 PM
NCT ID:
NCT00257803
Eligibility Criteria:
Inclusion Criteria:
* Aged 19 years or over
* Having a cesarean section
* Have one or more of the following
1. a larger than average uterus, because of
* a large baby
* twins, triplets, etc
* a large volume of fluid around the baby
2. have received oxytocin to help stimulate labor for eight or more hours before cesarean section
3. have infection inside the uterus that is treated with antibiotics
4. bleeding after giving prior birth
5. the placenta is in a position where it is more likely to bleed
6. have had five or more pregnancies before current one
Exclusion Criteria:
* Significant medical problem such that an oxytocin bolus might not be safe
* Active bleeding and their blood pressure or pulse rate are not normal
* Blood does not clot normally
* Aged less than 19 years
* Does not understand English
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
19 Years
Study:
NCT00257803
Study Brief:
Protocol Section:
NCT00257803