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Multi dimensional risk stratification study on re intervention of residual after induced abortion

Multi dimensional risk stratification study on re intervention of residual after induced abortion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123360
Enrollment
Unknown
Registered
2026-04-25
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

After an induced abortion, residual abortion tissue requires a second uterine curettage

Interventions

Residual secondary curettage group (case group) and residue-free control group (1:3 match):None

Sponsors

The First People's Hospital of Foshan
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients undergoing induced abortion in our hospital; 2. Complete postoperative follow-up data (including ultrasound and hCG records);

Exclusion criteria

Exclusion criteria: 1. Loss of follow-up or loss of key data > 20%; 2. Complicated with coagulation dysfunction or malignant tumor;

Design outcomes

Primary

MeasureTime frame
Need for second evacuation;Postoperative residual characteristics (size, location, vascularity);Postoperative HCG decline;—

Countries

China

Contacts

Public ContactZhu Minsan

The First People's Hospital of Foshan

zmshan@fsyyy.com+86 757 83162677

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026