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The Comparative evaluation of effect of Sublingual Misoprostol versus cervical misoprostol on second Trimester abortions

Phase 2
Recruiting
Conditions
Abortion.
Missed abortion
O02.1
Registration Number
IRCT20200127046280N2
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
200
Inclusion Criteria

Unifetal pregnancy
Missed abortion
Fetal malformations
Blighted ovum
Trisomies
Gestational age ( 12 weeks and less than 12 weeks )

Exclusion Criteria

Rupture of membrane
History of cesarean section more than once
History of allergy to misoprostol and prostaglandins
Contraindications of prostaglandin use ( like heart disease, kidney disease, history of seizures and hypotension )

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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