Uterine Fibroids in China: How Common They Are and What Increases Risk
Official title: Epidemiology and Risk Factors of Uterine Fibroids in China
Run by Tongji Hospital · NCT05840042 · Data updated 2026-11-12
This study tests how common uterine fibroids are in Chinese women and what factors relate to developing them and needing surgery.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 20000 (estimated) |
| Sponsor | Tongji Hospital Academic / other |
| Locations | 1 site (Wuhan, Hubei) |
| Status | Recruiting |
| Started | June 19, 2023 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | October 13, 2026 |
| Trial ID | NCT05840042 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women residing in China for at least 6 months who consent to participate and complete the questionnaire.
✕Probably not a fit
Individuals who do not have or develop fibroids or who do not participate may not benefit from any direct intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to determine the prevalence and incidence of uterine fibroids in Chinese women and to identify associated risk factors. It will collect questionnaire data from eligible participants to characterize symptoms, diagnosis, and treatment histories. The study does not involve an intervention and will analyze patterns to inform future research and public health understanding of fibroids in China.
Why it matters
Potential benefit: Results could improve understanding of who is at risk for fibroids and inform future prevention or screening strategies.
How similar studies have gone: Previous epidemiology studies have helped map fibroid prevalence, but this study focuses on a Chinese population and may add localized insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Current place of residence≥ 6 months; * No serious mental illness or mental abnormality; * Those who agree to participate in this survey and cooperate in completing the questionnaire. Exclusion Criteria: \-
Where it's running
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Huazhong University of Science and Technology
Wuhan, Hubei, China Recruiting
Study contacts
- Principal investigator: Shixuan Wang, Doctor — Huazhong University of Science and Technology
- Study coordinator: Wenwen Wang, Doctor
- Email: petrawang@163.com
- Phone: 15927167698
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Relugolix (Ryeqo) with low‑dose add-back hormones for uterine fibroids and endometriosis and its effects on blood clotting
This trial will test whether the GnRH antagonist Relugolix combined with low‑dose estradiol and progestin (Ryeqo) changes blood clotting markers in adult women treated for uterine fibroids or endometriosis.
-
Evaluating uterine fibroids using ultrasound techniques before and after treatment
This study is testing if a special ultrasound can help women with uterine fibroids see how their condition changes before and after a specific treatment called uterine artery embolization.
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Using Bearing nsPVA particles for treating uterine fibroids
This study is testing if a new type of particles used in a procedure can safely help women with painful uterine fibroids feel better.
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Impact of Uterine Fibroids on Women's Fertility
This study looks at how uterine fibroids might affect pregnancy rates in women aged 20-50 who are struggling with infertility.
-
Registry for pregnancy outcomes after Exablate treatment for uterine fibroids
This study is looking to see how the Exablate treatment for uterine fibroids affects pregnancy outcomes in people who have had the procedure.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.