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NCT07048327Recruiting

Cohort Study of Intrauterine Diseases

Source: ClinicalTrials.gov · Last updated 2 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

"This study employs a prospective cohort design by establishing a uterine cavity diseases research platform. The investigators will collect participants' current medical history, menstrual and obstetric history, past medical history, physical and gynecological examinations, imaging studies, laboratory tests, and pathological examinations. After the hysteroscopic surgery, the investigators will conduct a one-year follow-up on the disease progression of the participants. Through this comprehensive approach, the investigators aim to deeply investigate the pathogenesis, risk factors, and optimized treatment strategies for uterine cavity diseases."

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
19 Jun 2025
Start date
1 Jul 2025
Primary completion date
31 Jul 2028
Lead sponsor
Wenwen Wang
NCT number
NCT07048327

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 1 Jul 2025 to the primary completion date, 31 Jul 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent participation in other drug clinical trials;

Other

  • Contraindications to or inability to tolerate hysteroscopy/curettage procedures;
  • Unwilling or unable to provide informed consent;
  • Unwilling or unable to adhere to study protocols.

Who the study is looking for

  • Age: 18-80 years;
  • Patients requiring hysteroscopy or diagnostic curettage for intrauterine pathologies (e.g., endometrial hyperplasia, endometrial polyps, submucosal uterine fibroids, adenomyosis, or endometrial malignancies);
  • Willing and able to comply with follow-up requirements;
  • Signed informed consent obtained.

Age in the registry: 18 years to 80 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Coordinator of this site? Confirm its status
WuhanChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.