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 @ 3:52 AM
Ignite Modification Date:
2025-12-25 @ 3:52 AM
NCT ID:
NCT06225102
Eligibility Criteria:
Inclusion Criteria:
* be between the ages of 18-25
* Giving 6 points or more to the least menstruation pain on the day that individuals experience the most severe dysmenorrhea symptoms (VAS) out of 10 points on the VAS Visual Pain Scale
* Being Nulliparous (never giving birth)
* Regular menstruation for the last six months
* Not having any gynecological diagnosis
* Not having had a gynecological operation
* Volunteering to participate in the study
Exclusion Criteria:
* Being a man
* Being married
* Being diagnosed with secondary dysmenorrhea
* Giving menstruation pain less than 6 points out of 10 on the VAS Visual Pain Scale.
* Taking painkillers 12 hours before the assessments.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
25 Years
Study:
NCT06225102
Study Brief:
Protocol Section:
NCT06225102