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 @ 10:55 PM
Ignite Modification Date:
2025-12-24 @ 10:55 PM
NCT ID:
NCT05081869
Eligibility Criteria:
Inclusion Criteria:
* Being a nulliparous woman between the ages of 18-35,
* Having a primary dysmenorrhea symptom,
* Having a regular menstrual cycle (28 ± 7 days),
* Menstrual pain Visual Analogue Scale score higher than 4 cm in the last 6 months
Exclusion Criteria:
* Having gastrointestinal, urogynecological, autoimmune, psychiatric, neurological diseases or other chronic pain syndromes,
* To have given birth, Current pregnancy status,
* Using an intrauterine device and having had pelvic surgery,
* Using drugs including oral contraceptives or antidepressants at least 6 months before the study,
* Having an irregular menstrual cycle (those with a menstrual cycle shorter than 21 days or longer than 35 days)
* A pathological history or ultrasonographic result showing secondary dysmenorrhea.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT05081869
Study Brief:
Protocol Section:
NCT05081869