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 @ 11:03 PM
Ignite Modification Date:
2025-12-24 @ 11:03 PM
NCT ID:
NCT05328869
Eligibility Criteria:
Inclusion Criteria:
* Women with primary dysmenorrhea complaint according to the Primary Dysmenorrhea Consensus Guide,
* Over 18 years of age,
* Having a mean pain intensity of moderate and higher according to the Visual Analogue Scale in the last 6 months,
* Having a regular menstrual cycle (28±7 days),
* Volunteered to participate in the study.
Exclusion Criteria:
* Having a pathological history and radiological findings pointing to secondary dysmenorrhea,
* Using oral contraceptives/antidepressants at least 6 months,
* Receiving hormone therapy,
* Undergoing pelvic surgery,
* Pregnant,
* Giving birth,
* Using an intrauterine device,
* Having neurological, orthopedic and/or rheumatological diseases
* Having a psychiatric disease,
* Having a history of malignancy
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05328869
Study Brief:
Protocol Section:
NCT05328869