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Establishment and Application of Key Technology System for Uterine Cavity Regeneration and Repair

Establishment and Application of Key Technology System for Uterine Cavity Regeneration and Repair

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300079136
Enrollment
Unknown
Registered
2023-12-26
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Intrauterine adhesion

Interventions

Observation group (Sampling 0.5g endometrial tissue for in vitro seperation and culture):None

Sponsors

Women's Hospital School of Medicine Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Age 20-40 years old 2. First time diagnosis with moderate to severe intrauterine adhesion (AFS score>5) or with recurrent intrauterine adhesion or with thin endometrium

Exclusion criteria

Exclusion criteria: 1. Received G-CSF treatment (including subcutaneous injection or intrauterine infusion) in the past 3 months; 2. Combined with endometrial polyps; 3. Combined with endometrial hyperplasia or endometrial malignancy; 4. Patients who are participating in other clinical studies; 5. Other reasons that the investigator considers unsuitable for clinical investigators;

Design outcomes

Primary

MeasureTime frame
proliferation of endometrial cell;

Countries

China

Contacts

Public ContactYue Wang

Women's Hospital School of Medicine Zhejiang University

misswangyue@zju.edu.cn+86 137 7786 2608

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026