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The effect of misoprostol with isosorbide mononitrate on the induction of first-trimester abortio

Phase 2
Recruiting
Conditions
Therapeutic Abortion.
Therapeutic/Medical Abortion (termination of pregnancy)
Registration Number
IRCT20130812014333N138
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
54
Inclusion Criteria

Nullipara and multipara to 5 Parity and singleton women
No history of previous cesarean section and uterine surgery

Exclusion Criteria

Women with the open cervix and contraindication for isosorbide mononitrate (IMN)
Women with significant heart disease or anemia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time of cervical opening from induction onset. Timepoint: 24 hours after the end of the study. Method of measurement: Doctor Observation.;Secretion time of pregnancy products from onset of induction. Timepoint: 24 hours after the end of the study. Method of measurement: Doctor Observation.;Complete abortion. Timepoint: 24 hours after the end of the study. Method of measurement: Doctor Observation.
Secondary Outcome Measures
NameTimeMethod
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