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 @ 11:35 PM
Ignite Modification Date:
2025-12-24 @ 11:35 PM
NCT ID:
NCT00488956
Eligibility Criteria:
Inclusion Criteria:
1. Women with a singleton pregnancy;
2. Undergoing an elective CD under regional anesthesia (spinal or combined spinal epidural (CSE);
3. Normotensive; and
4. At least 37 weeks gestation
Exclusion Criteria:
1. Reasons for potential excessive blood loss (e.g. placenta previa);
2. Reasons for potential uterine atony and above average use of oxytocin (e.g. multiple pregnancies, polyhydramnios);
3. Non lower segment uterine incision;
4. Renal or cardiac disease;
5. Use of diuretics; or
6. Open wounds on the right foot and ankle.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00488956
Study Brief:
Protocol Section:
NCT00488956