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 @ 2:56 PM
Ignite Modification Date:
2025-12-24 @ 2:56 PM
NCT ID:
NCT06741059
Eligibility Criteria:
Inclusion Criteria:
* Aged 18 and above
* Have regular menstrual cycles (lasting 3 to 8 days, with a menstrual cycle range of 21 to 35 days)
* Have dysmenorrhea pain severity rated 4 or higher on the Visual Analog Scale (VAS)
Exclusion Criteria: Women with the following conditions were excluded from the study:
* Secondary dysmenorrhea
* Using oral contraceptives
* Having impaired tissue integrity in the abdominal area
* Having previous experience with TENS
* Having a history of nerve damage or sensory loss
* Having a pacemaker
* Having any systemic diseases
* Being pregnant or in the postpartum period
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06741059
Study Brief:
Protocol Section:
NCT06741059