The effect of vaginal misoprostol and isosorbide mononitrate on under 20 week miscarriages

Phase 3

Recruiting

• Conditions: Cervix Preparation for Abortion.; Missed abortion; O02.1

• Registration Number: IRCT20190901044658N1
• Lead Sponsor: Ardabil University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

Gestational age under 20 weeks
candidate for abortion due to proved fetal death confirmed by sonography
severe abnormality in which the fetus is not viable

Exclusion Criteria

Certain underlying disease such as cancer

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The time of the cervix preparation for abortion. Timepoint: The patient will be examined regularly every 6 hours, and if the fetus is not discharged, the drug will be repeated after 6 to 12 hours. Method of measurement: It will be a clinical and cervical examination by a resident resident.