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:
2025-12-25 @ 5:02 AM
Ignite Modification Date:
2025-12-25 @ 5:02 AM
NCT ID:
NCT05251818
Eligibility Criteria:
Inclusion Criteria:
* Between the ages of 18-35,
* Having a cesarean section with general anesthesia,
* After the operation, non-narcotic and the same type of analgesic substance is applied to provide pain control,
* Able to speak and understand Turkish,
* Postpartum women with at least primary school graduates will be included in the study.
Exclusion Criteria:
* Being obese (BMI≥30),
* Opioid medication given in the post-op period,
* Any disease related to the digestive system,
* Having a history of abdominal surgery,
* Chronic constipation or irregularity in defecation habits,
* Having any chronic disease (such as diabetes, hypertension, heart failure),
* Pregnancy complications (such as preeclampsia, gestational diabetes),
* The baby is in the intensive care unit,
* Having any physical problem that will prevent the application of acupressure to LI4 and TH 6 points,
* Women who develop disorders or insufficiency related to fluid-electrolyte balance, acid-base balance and tissue perfusion during and after the operation will not be included in the study.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT05251818
Study Brief:
Protocol Section:
NCT05251818