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efficacy of misoprostol on abortion therapy

Not Applicable
Conditions
abortion therapy.
Medical abortion
Registration Number
IRCT2013090414563N1
Lead Sponsor
Golestan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
70
Inclusion Criteria

The inclusion criteria : pregnant women undergoing therapeutic abortion; aged 15 to 35 years; satisfaction of the trial conducted in this study.

The exclusion criteria : previous cesarean section; previous uterine Myomectomy;allergies and contraindications for the use of prostaglandins;vaginal bleeding before treatment; or rupture of Mambrane or vaginitis before treatment ;dissatisfaction upon entering the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Abortion therapy. Timepoint: per 6 hours to 48 hours. Method of measurement: Bougie#(6) passed through the cervix.
Secondary Outcome Measures
NameTimeMethod
Interval between administration of the drug to induce abortion. Timepoint: Interval between Putting tablets in the vagina to induce abortion. Method of measurement: Per hour.;Adverse Drug Reactions. Timepoint: when The problem occurred. Method of measurement: researcher Find.;Indication of abortion. Timepoint: when hospitalization. Method of measurement: The researcher identified.
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