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COMPARISON OF TWO DRUG REGIMEN FOR TREATMENT OF EARLY PREGNANCY FAILURE

Not Applicable
Conditions
Health Condition 1: null- Patients with early pregnancy failure
Registration Number
CTRI/2013/03/003492
Lead Sponsor
niversity College of Medical Sciences and Guru Teg Bahadur Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
92
Inclusion Criteria

Women with early pregnancy failure less than or equal to 12 weeks.

Exclusion Criteria

1. Incomplete abortion as defined as open cervix and large amount of cramping / bleeding.

2. Hemodynamic instability / heavy vaginal bleeding.

3. Hemoglobin less than or equal to 8 g%.

4. Inability to follow-up (i.e. lack of transportation / access to telephone).

5. Bleeding disorder / taking anticoagulants.

6. Obvious infection.

7. Allergy to mifepristone / misoprostol.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eed for surgical evacuationTimepoint: 14 days post intervention
Secondary Outcome Measures
NameTimeMethod
Emergency admission rate, blood transfusion rate, side effects, number of women who would choose medical management in futureTimepoint: 14 days post intervention
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