A clinical trial to study the effects of mifepristone and misoprostol given at same time for abortion.
Phase 3
Completed
- Conditions
- Health Condition 1: null- Medical abortion in less than 10 weeks of pregnancy
- Registration Number
- CTRI/2010/091/001422
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Prescence of intrauterine pregnancy
Gestational age not exceeding 63 days at administration of Mifepristone
Aged >16 yrs
Willingness to comply with schedule of follow up visits
Exclusion Criteria
Ectopic Pregnancy
Systemic corticosteroid therapy
Adrenal sufficiency
Asthma
Glaucoma
Poorly controlled seizures
Hb <10 gm%
Coagulopathy
Anticoagulant therapy
Pregnancy with intrauterine device in situ
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success of Medical abortionTimepoint: 14 days
- Secondary Outcome Measures
Name Time Method Compare the efficacy of concurrent protocol with 48 hours protocolTimepoint: 14 days