Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
ID06982989

Clinical Study on the Treatment of Pelvic Pain With Wearable Dual-band LED Device

Led by Peking University Third Hospital · Updated on 2025-05-21

250

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a prospective clinical trial to study female pelvic pain, including dysmenorrhea and chronic pelvic pain. The study aims to identify suitable participants and evaluate the effects of a wearable dual-band LED device on pelvic pain and related blood markers. This investigation is sponsored by Peking University Third Hospital and focuses on non-menstrual periods for treatment. Participants will use the dual-band LED device to deliver low-dose phototherapy to the pelvic area and specific acupoints. The treatment is self-selected by patients who choose to use the LED device for their pelvic pain. The study does not involve placebo or control groups and does not use masking or blinding. During the study, participants will be monitored for changes in pelvic pain and serological indicators. The primary outcome is the effectiveness of the LED treatment one month after therapy. Participants will be followed over the course of the trial, which runs until December 31, 2028. Assessments will include clinical observations and relevant blood tests to evaluate treatment impact.

CONDITIONS

Brief Title

Clinical Study on the Treatment of Pelvic Pain With Wearable Dual-band LED Device

Who Can Participate

Age: 18Years - 35Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pelvic pain
Not Eligible

You will not qualify if you...

  • Irregular menstrual cycles
  • Inflammatory disease
  • Pregnant
  • Light allergy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 1 month

Participants use a wearable dual-band LED device to treat pelvic pain.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 1 location

1

Peking Unniversity Third Hospital

Beijing, Beijing Municipality, China, 100191

Actively Recruiting

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Research Team

Z

Zhangxin Wu

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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