Clinical Study on the Treatment of Pelvic Pain With Wearable Dual-band LED Device
Not Applicable
Recruiting
- Conditions
- Pelvic Pain
- Registration Number
- NCT06982989
- Lead Sponsor
- Peking University Third Hospital
- Brief Summary
This study is a prospective clinical trial, which intends to prospective include female pelvic pain (dysmenorrhea and chronic pelvic pain), screen suitable cases, wear dual-band LED devices in non-menstrual period, perform low-dose phototherapy on local pelvic area and acupoints, and observe the changes of pelvic pain and related serological indicators in clinical practice.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 250
Inclusion Criteria
- pelvic pain
Exclusion Criteria
- Irregular menstrual cycles;
- Inflammatory disease;
- pregnant;
- Light allergy;
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Efficacy that LED release pelvic pain 1 month after the treatment Use VAS scale to evaluate the pain.The changes in the VAS score of pelvic pain before and after treatment.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Peking Unniversity Third Hospital
🇨🇳Beijing, Beijing, China