NCT07592403Recruiting
Efficacy of Pulsed Electromagnetic Field Therapy on Women With Endometriosis
Efficacy of Pulsed Electromagnetic Field Therapy on Women With Endometriosis, A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 19 May 2026
Brief summary (registry, in English)
This randomized, sham-controlled, double-blinded clinical trial aims to investigate the effects of pulsed electromagnetic field therapy (PEMF) on pain intensity, quality of life, and pelvic floor morphometric changes assessed by four-dimensional trans perineal ultrasound (4D TPUS) in women diagnosed with endometriosis. Participants will be randomly allocated into either a PEMF therapy group or a sham PEMF control group. Both groups will continue receiving stable standard medical care throughout the study period. Assessments will be conducted at baseline, after completion of the 8-week intervention period, and at 3-month follow-up.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 11 May 2026
- Start date
- 16 May 2026
- Primary completion date
- 20 Jan 2027
- Lead sponsor
- Beni-Suef University
- Diseases
- Endometriosis
- NCT number
- NCT07592403
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 16 May 2026 to the primary completion date, 20 Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous pelvic surgery within the past 6 months
- Participation in another clinical trial during the previous 3 months
- Contraindications to electromagnetic therapy
Other illness
- History of gynecological or pelvic malignancy
- Active pelvic inflammatory disease or acute pelvic infection
- Neurological, rheumatological, or severe musculoskeletal disorders affecting assessment procedures
Other
- Pregnancy or planned pregnancy during the study period
- Implanted electronic medical devices such as pacemakers or neurostimulators
Who the study is looking for
- Women aged 18 to 45 years
- Clinically, radiologically, or laparoscopically diagnosed endometriosis
- Chronic pelvic pain persisting for at least 6 months
- Stable pharmacological or hormonal treatment for at least 3 months before enrollment
- Ability to understand study procedures and provide written informed consent
Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Outpatient clinic, faculty of Physical Therapy, Beni Suef University Coordinator of this site? Confirm its status | Banī Suwayf | Egypt | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.