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Efficacy assessment of acupuncture in improving symptoms of Uterine fibroids: a randomized controlled trial

Efficacy assessment of acupuncture in improving symptoms of Uterine fibroids: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030438
Enrollment
Unknown
Registered
2020-03-01
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Uterine fibroids

Interventions

Sponsors

Fuzhou hospital of traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 18-55 years; 2. Meet the western medical diagnostic standards for uterine fibroids; 3. Patients with the uterine body not exceed 10 weeks of pregnancy size, tumor diameter <5cm; 4. Patients who did not use other drugs that had an impact on the results of this study within 1 month before enrollment; 5. Patients willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with ovarian tumors, adenomyosis, uterine malignant tumors, and urinary tract infections; 2. Pregnant or lactating women; 3. Patients who have taken hormonal drugs in the past 3 months, or have been treated with this research protocol; 4. With severe heart, liver and kidney dysfunction, mental disorders; 5. Subjects who are participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Uterine Fibroid Symptom Severity Scale(SS-QOL);Uterine fibroids symptoms and health-related quality of life questionnaire (HR-QOL);Traditional Chinese medicine syndrome score;

Countries

China

Contacts

Public ContactMinqin Zheng

Fuzhou hospital of traditional Chinese medicine

caiweng12@sina.com+86 591-87678520

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026