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 @ 4:56 AM
Ignite Modification Date:
2025-12-25 @ 4:56 AM
NCT ID:
NCT05962918
Eligibility Criteria:
Inclusion Criteria:
* Having no complications for vaginal delivery
* Having no dystocia affecting the birth process (e.g., prolonged labor, precipitate labor, shoulder dystocia)
* Having a singleton pregnancy,
* Having a fetal head with an anterior cephalic position,
* Being at the latent phase of labor,
* Having no perineal scar tissue,
* Having no diagnosis of vaginal fungus or infection,
* Having a fetus with a birth weight between 2500 and 4000 g,
* Having no communication problems.
Exclusion Criteria:
-All pregnant women who developed fetal distress during labor or had to undergo cesarean delivery were excluded from the study.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT05962918
Study Brief:
Protocol Section:
NCT05962918