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Prospective observational Real-World study of retained products of conception

Prospective observational Real-World study of retained products of conception

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060812
Enrollment
Unknown
Registered
2022-06-12
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

retained products of conception

Interventions

None listed

Sponsors

The Third Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Clinical diagnosis of intrauterine pregnancy residue, and ultrasound suggested the maximum diameter of the lesion of 0.5cm

Exclusion criteria

Exclusion criteria: 1.Active bleeding requires immediate surgical intervention; 2.Wwith obvious infection; 3.With severe organ insufficiency, including coagulation dysfunction.

Design outcomes

Primary

MeasureTime frame
Incidence of intrauterine adhesions;—

Secondary

MeasureTime frame
The number of operations;Endometrial thickness after treatment;pregnancy rate;spontaneous abortion rate;live birth rate;—

Countries

China

Contacts

Public ContactXU Dabao

The Third Xiangya Hospital of Central South University

13017386201@126.com+86 13017386201

Outcome results

None listed

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