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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06982989
Enrollment
250
Registered
2025-05-21
Start date
2023-01-01
Completion date
2028-12-31
Last updated
2025-05-21

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

Conditions

Pelvic Pain

Keywords

LED, pelvic pain

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.

Interventions

DEVICEuse LED to treat pelvic pain

Use led to treat pelvic pain

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* pelvic pain

Exclusion criteria

* Irregular menstrual cycles; * Inflammatory disease; * pregnant; * Light allergy;

Design outcomes

Primary

MeasureTime frameDescription
Efficacy that LED release pelvic pain1 month after the treatmentUse VAS scale to evaluate the pain.The changes in the VAS score of pelvic pain before and after treatment.

Countries

China

Contacts

Primary ContactZhangxin Wu
wzxpku2008@126.com82267518

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026