Primary Dysmenorrhea Clinical Trial
Official title:
The Role of Transcutaneous Electrical Nerve Stimulation (TENS) for Menstrual Pain Relief: A Randomized Control Trial
NCT number | NCT05178589 |
Other study ID # | HS-21-00629 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 1, 2022 |
Est. completion date | May 1, 2023 |
Verified date | October 2023 |
Source | University of Southern California |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study aims to verify the analgesic potential of a transcutaneous electrical nerve stimulation (TENS) device using patients with primary dysmenorrhea and compare it with a control period without usage.
Status | Completed |
Enrollment | 44 |
Est. completion date | May 1, 2023 |
Est. primary completion date | April 27, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - History of lower abdominal pain (dysmenorrhea) for more than 6 consecutive menstrual cycles with a moderate or severe pain rating =5 out of 10 over course of last year - BMI of 18.5-29.9 as a BMI below or above these cut points results in highly varied menstrual cycle lengths - Not taking contraception or other types of medication that could influence reproductive status - Regular menstruation - Medically free from chronic diseases - Free from known gynecological problems (ie. Endometriosis, Fibroids, Ovarian Cysts) - History of analgesic pill intake during menstruation - No pelvic pathology Exclusion Criteria: - Amenorrhea - On a form of contraception - Secondary dysmenorrhea and/or other gynecological problems that may cause pain - No discomfort, pain, or other symptoms during menstruation - History of surgery over lower abdomen area - Allergy to ibuprofen - Cardiac disability - Pacemaker - Arterial disease - Uncontrolled hemorrhage - Blood clots - Pregnancy or trying to become pregnant - Cancerous lesions - Exposed metal implants - History of seizures - Sensory or mental impairment - Unstable fractures |
Country | Name | City | State |
---|---|---|---|
United States | University of Southern California Health Sciences Campus Center for Health Professions | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of Southern California |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | The surface area of TENS pain relief | Participants will use either one or 2 unit TENS. | 1 month | |
Primary | Analgesic effects of TENS on primary dysmenorrhea. | To determine whether TENS will reduce pain symptoms in those with primary dysmenorrhea. Subjective pain will be assessed using an 11 point visual analog scale (VAS). The scale ranges from 0 to 10, with 0 being no pain and 10 being maximum pain. | 1 month | |
Secondary | Change in analgesic pill consumption during menstruation | Participants will be administered a daily survey where they will be asked to record analgesic pill intake throughout the day. | 1 month |
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