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A randomised, controlled clinical trial involving women who have aborted spontaneously; the health, social and operational costs, outcomes of conservative and routine management

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43067169
Enrollment
Unknown
Registered
2002-10-10
Start date
1995-10-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Spontaneous abortion Pregnancy and Childbirth Spontaneous abortion

Interventions

Routine surgical evacuation or medical evacuation of the uterus using misoprostol

Sponsors

Hong Kong Health Services Research Fund (Hong Kong)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All women admitted to the gynaecological unit of the Prince of Wales Hospital from October 1995 to January 1998 with: 1. A clinical diagnosis of spontaneous abortion 2. A positive urinary pregnancy test, and 3. Transvaginal Sonography (TVS) evidence of retained Products Of Conception (POCs)

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

Hong Kong

Outcome results

None listed

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