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 @ 11:05 PM
Ignite Modification Date:
2025-12-24 @ 11:05 PM
NCT ID:
NCT06146569
Eligibility Criteria:
Inclusion Criteria:
* Being diagnosed with PD according to the No. 345 Primary Dysmenorrhea Consensus Guidelines,
* An NRS score of at least three during menstruation before treatment,
* Being a woman between the ages of 18-40,
* A regular menstrual cycle of 28±7 days,
* Being nulliparous,
* No history of brain surgery, tumour or intracranial metal implantation,
* No chronic genitourinary infection or alcohol or drug use.
Exclusion Criteria:
* History of dizziness or epileptic disease,
* Pregnancy,
* Women with intrauterine devices,
* Metal implants in the head area,
* Women with skin lesions in the area where the electrodes will be placed,
* Use of analgesic drugs during treatment,
* Women with neurological or heart disease,
* Women are diagnosed with gynaecological conditions (endometriosis, adenomyosis, uterine fibroids, etc., which may be associated with secondary dysmenorrhea).
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT06146569
Study Brief:
Protocol Section:
NCT06146569