Actively Recruiting

Age: 18Years - 80Years
FEMALE
NCT07048327

Cohort Study of Intrauterine Diseases

Led by Wenwen Wang · Updated on 2025-07-02

2000

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

"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."

CONDITIONS

Official Title

Cohort Study of Intrauterine Diseases

Who Can Participate

Age: 18Years - 80Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years
  • Patients requiring hysteroscopy or diagnostic curettage for intrauterine pathologies such as endometrial hyperplasia, endometrial polyps, submucosal uterine fibroids, adenomyosis, or endometrial malignancies
  • Willing and able to comply with follow-up requirements
  • Signed informed consent obtained
Not Eligible

You will not qualify if you...

  • Concurrent participation in other drug clinical trials
  • Contraindications to or inability to tolerate hysteroscopy or curettage procedures
  • Unwilling or unable to provide informed consent
  • Unwilling or unable to adhere to study protocols

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China, 430000

Actively Recruiting

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Research Team

W

Wen W Wang, Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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