Clinical Study on the Treatment of Pelvic Pain With Wearable Dual-band LED Device
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: use LED to treat pelvic pain.
- Who it may be relevant to
- Registry conditions: Pelvic Pain. Basic parameters: 18 years — 35 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Device use LED to treat pelvic pain
Use led to treat pelvic pain
Primary outcome measures
- Efficacy that LED release pelvic pain [Time frame: 1 month after the treatment]
Eligibility criteria
Inclusion criteria
- pelvic pain
Exclusion criteria
- Irregular menstrual cycles;
- Inflammatory disease;
- pregnant;
- Light allergy;
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
China · 1 center
- Peking Unniversity Third Hospital — Beijing
Identifiers
NCT: NCT06982989 · LED Pelvic pain · 2022YFB3604705