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:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-26 @ 3:18 PM
NCT ID:
NCT07323758
Eligibility Criteria:
Inclusion Criteria:
* Study participation criteria
* Women aged 18-49,
* Primiparous,
* Having a medio-lateral episiotomy,
* Having a singleton pregnancy,
* Vertex presentation,
* Having given birth vaginally,
* Having an episiotomy length of 4-5 cm,
* Having an uncomplicated newborn,
* Volunteering to participate in the study,
* Being able to speak and understand Turkish.
Exclusion Criteria:
* Women who experienced deep lacerations (anal sphincter injuries, 3rd and 4th degree lacerations) during labor,
* Those who underwent operative delivery (with vacuum or forceps),
* Those with visual, hearing, or sensory impairments,
* Those who were not diagnosed with a psychiatric disorder but had problems,
* Those diagnosed with a high-risk pregnancy,
* Those who had any signs of infection, such as vaginal redness or swelling,
* Those who developed complications during any stage of labor,
* Women with chronic illnesses (diabetes mellitus, thyroid disease, and hypertension) will not be included in the study.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT07323758
Study Brief:
Protocol Section:
NCT07323758