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Misoprostol mifepristone for termination of pregnancy

Efficacy of misoprostol administration 24 hours after mifepristone for termination of pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/07/001894
Enrollment
200
Registered
2011-07-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Medical termination of pregnancy

Interventions

Intervention1: Mifepristone followed by Misoprostol after 24 hours: Mifepristone 200 mg orally followed by 400 microgram of Misoprostol per vaginally after 24 hours Control Intervention1: Mifepristone

Sponsors

Indian Council Of Medial Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Intrauterine pregnancy 2. Willing for compliance and follow-up 3. Gestational age less than 9 weeks

Exclusion criteria

Exclusion criteria: 1. Ectopic pregnancy 2. Breast feeding 3. Systemic steroids 4. Adrenal insufficiency 5. Bronchial asthma 6. Glaucoma

Design outcomes

Secondary

MeasureTime frame
Side effects of the regimenTimepoint: All the adverse reactions/ effects till 14 days of stopping therapy—

Primary

MeasureTime frame
Efficacy of misoprostol administration 24 hours after mifepristone for early medical abortionTimepoint: Efficacy of misoprostol administration 24 hours after mifepristone for early medical abortion—

Countries

India

Contacts

Public ContactManju Lata Verma
gaganmlv@gmail.com

Outcome results

None listed

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