CTRI/2018/01/011157
Completed
未知
A prospective comparative study of mifepristone followed by misoprostol or ethacridine lactate and oxytocin for second trimester abortions
Project in the Department of Obstetrics and Gynecology0 sites120 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- SECOND TRIMESTER ABORTIONS
- Sponsor
- Project in the Department of Obstetrics and Gynecology
- Enrollment
- 120
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Second trimester abortions for medical, social, eugenic reasons
- •2\.Intrauterine pregnancy
- •3\.18\-40 years
- •4\.Consent to participate in the study
Exclusion Criteria
- •1\.Less than 13 weeks and more than 20 weeks pregnancy terminations
- •2\.Patients with history of renal disease or hepatic disease or bronchial asthma or hematological disease or glaucoma or heart disease etc
- •3\.Hemoglobin less than 10 gm/dl
- •4\.Patients with previous caesarean section and other uterine scars
- •5\.Symptomatic reproductive tract infections
- •6\.Hypersensitivity to mifepristone or misoprostol or ethacridine lactate or oxytocin
- •7\.Rupture of membranes
Outcomes
Primary Outcomes
Not specified
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