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A prospective, randomized, double-blind, parallel, placebo-controlled, multicenter clinical study of acupoint application in the treatment of endometriosis

A prospective, randomized, double-blind, parallel, placebo-controlled, multicenter clinical study of acupoint application in the treatment of endometriosis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005686
Enrollment
Unknown
Registered
2022-03-08
Start date
2022-03-15
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Endometriosis

Interventions

Control Group:Acupoint application of placebo patch with placebo treatment
Experimental group:Acupoint application, detumescence and pain relief combined with traditional Chinese medicine

Sponsors

Affiliated Hospital of Shandong University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of endometriosis; 2. Age 18-45, menstrual cycle 21-35 days, period 3-7 days; 3. Patients with mass diameter < 4 cm; 4.35IU/L < serum CA125 < 80IU/L; 5. Informed consent and signing of informed consent.

Exclusion criteria

Exclusion criteria: 1. Dysmenorrhea caused by various primary dysmenorrhea or other diseases; 2. Have accepted other new drug clinical experimenter in recent 3 months; 3. People with coagulation disorder; 4. People who have been allergic to multiple drugs or have an allergic constitution; 5. Persons with combined mental illness, alcoholism and/or psychoactive substance substance abuse and dependence; 6. Patients with skin trauma, ulcers, skin infection or scar at the application site and those who are allergic to the patch; 7. Pregnant or lactating women. Note: any one or more of the above items should be excluded and cannot be selected.

Design outcomes

Primary

MeasureTime frame
Uterine size, mass size;Dysmenorrhea symptom score;CA125;Dysmenorrhea pain score;

Countries

China

Contacts

Public ContactSunzhengao
sunzhengao77@126.com13708938621

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026