Status:
UNKNOWN
Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Women
Lead Sponsor:
Aswan University Hospital
Conditions:
IUCD Complication
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
To compare the effect of vaginal dinoprostone versus vaginal misoprostol administered before the copper intrauterine device(IUD) insertion in reducing IUD insertion pain and the difficulty in insertin...
Detailed Description
Long-acting reversible contraception methods are highly effective methods for reduction of the unplanned pregnancy rate worldwide. The intrauterine device is a single procedure that provides reliable,...
Eligibility Criteria
Inclusion
- multi parous women requesting copper IUD insertion
- body mass index more than 25
Exclusion
- pregnancy,
- null parous women,
- contraindications or allergy to dinoprostone or misoprostol,contraindication to IUD insertion,
- untreated active cervicitis or vaginitis,
- undiagnosed abnormal uterine bleeding
Key Trial Info
Start Date :
September 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 30 2021
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT04505917
Start Date
September 1 2020
End Date
August 30 2021
Last Update
August 18 2020
Active Locations (1)
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1
Aswan University Hospital
Aswān, Egypt, 81528