The Clinical Efficacy Observation of CO2-Laser-Moxibustion in Treating Endometriosis Related Chronic Pelvic Pai

Phase 1

Recruiting

• Conditions: endometriosis related chronic pelvic pain

• Registration Number: ITMCTR1900002429
• Lead Sponsor: Pudong New Area TCM Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. Female patients aged between 20-50 years;
2. meet the diagnostic criteria for endometriosis recommended by the Chinese Medical Association Obstetrics and Gynecology Branch Guidelines (2015);
3. have no pelvic nodules or uterine adnexa mass, or have lesion with diameter=4cm; 3).have no fertility needs, no intention to use hormone therapy;
4. agree to use the analgesic or non-steroidal anti-inflammatory drug, such as pain control, only under the guidance of a specialist in obstetrics and gynecology and will not change the regimen without permission;
5. meet the criteria for the qi and blood stasis type, or cold and damp stagnation type, or qi and blood deficiency type, or liver and kidney deficiency;
6. Volunteer to participate in this topic and sign the informed consent form.

Exclusion Criteria

1. have any test drug or hormonal drug therapy has been used in the past 30 days;
2. have the imaging examination or pathological examination which suggest other tumor or cancer;
3. pregnant or lactate woman;
4. have disease that might influence the participation and the completion of the study, such as myocardial infarction or stroke, congestive heart failure, severe chronic obstructive pulmonary disease, cancer, diabetes, severe systemic disease, and severe mental illness in the past 3 months,local skin scars;
5. have medical history of infection or herpes in the treatment area; history of photosensitive dermatitis;
6. have participation of any participants-blinded laser moxibustion trial or simultaneous participation of any other research during this trial period;
7. are not willing to be randomly assigned.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Gracely Box Scale;

Secondary Outcome Measures

Name	Time	Method
records of application NSAIDs;visual analogue scale;