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A multi-center randomized controlled clinical study of HIFU combined with Guizhi Poria Capsule in sequential treatment of uterine fibroids

Phase 4
Recruiting
Conditions
intramural uterine fibroids, IUF
Registration Number
ITMCTR2100005040
Lead Sponsor
Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

1. Aged 20 to 49 years, regular menstrual cycle, 21-35 days;
2. Those who meet the IUF diagnostic criteria and the diameter of fibroids is <=8cm and >=3cm;
3. Those who meet the conditions of HIFU treatment and receive HIFU treatment;
4. Those who have no requirement for childbirth during treatment;
5. Subjects gave informed consent and signed an informed consent form voluntarily.

Exclusion Criteria

1. Those who are allergic to the relevant drug ingredients in this study;
2. Patients with severe primary diseases and mental illnesses such as severe heart, cerebrovascular, liver, kidney and hematopoietic system, diabetes, and thyroid diseases;
3. Submucosal fibroids, subserosal fibroids, adenomyosis, adenomyoma, and malignant transformation;
4. Those who have participated in other clinical researches within the past month, or are using similar drugs and related treatments within one month, and the efficacy of the drugs is difficult to judge;
5. The investigator believes that it is not suitable to participate in this clinical research.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
terine size;Chinese Medicine syndrome score;Uterine fibroids size;
Secondary Outcome Measures
NameTimeMethod
terine Fibroids Symptoms and Health-Related Quality of Life Questionnaire;
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