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A single-center randomized controlled trial of magnetic stimulation in the treatment of pelvic floor myofascial pain syndrome

A single-center randomized controlled trial of magnetic stimulation in the treatment of pelvic floor myofascial pain syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061883
Enrollment
Unknown
Registered
2022-07-06
Start date
2022-07-05
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic floor myofascial pain syndrome

Interventions

Magnetic stimulation treatment group:Pelvic floor magnetic stimulation therapy
Control group:Pelvic floor pseudomagnetic stimulation therapy

Sponsors

The Seventh Affiliated Hospital of Sun Yat sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 year female with sexual life history, without cognitive impairment, and can understand and complete treatment projects; 2. Diagnosed as pelvic floor myofascial pain syndrome and no definite pathological changes were found by pelvic floor ultrasound; 3. Did not receive any relevant treatment 3 months before the visit; 4. No serious internal and external diseases; 5. Obtain informed consent

Exclusion criteria

Exclusion criteria: 1. Complicated with vaginal bleeding and acute pelvic inflammatory disease; 2. Pregnancy, malignant tumor, radiotherapy and chemotherapy; 3. Patients with cardiac pacemaker, defibrillation cardioverter and metal intrauterine device; 4. Patients with severe cardiopulmonary insufficiency, liver failure and bleeding tendency; 5. Nervous system diseases (such as stroke, epilepsy, Parkinson's disease, multiple sclerosis); 6. People who are allergic to magnetic stimulation; 7. Those who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
VAS (Visual Analogue Scale/Score) score changes of pelvic floor muscle tenderness before and after treatment;

Secondary

MeasureTime frame
VAS (Visual Analogue Scale/Score) score changes of subjective pain of patients before and after treatment;Glazer EMG evaluation before and after treatment results;Hypoechoic nodule in pelvic floor ultrasonic examination at pelvic floor tenderness points before and after treatment and the change of nodule size before and after treatment;Changes in the number of hypoechoic nodules at the tenderness points of the pelvic floor examined by pelvic ultrasound before and after treatment;Changes in the questionnaire of pelvic floor muscle dysfunction before and after treatment (PFDI-20);Changes of female sexual function index (FSFI score) before and after treatment;Changes of urinary incontinence before and after treatment;

Countries

China

Contacts

Public ContactLi Tian

The Seventh Affiliated Hospital of Sun Yat sen University

sandylitian@126.com+86 13902306411

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026