Status:
UNKNOWN
Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Women Delivered Only by Cesarean Delivery
Lead Sponsor:
Cairo University
Conditions:
IUD Pain
Eligibility:
FEMALE
18-45 years
Phase:
PHASE4
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
- women delivered only by elective cesarean section and not received analgesics in the last 24 hours
Exclusion
- contraindications to dinoprostone or misoprostol or IUD insertion and allergy to study drugs.
Key Trial Info
Start Date :
September 10 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 5 2019
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT04080349
Start Date
September 10 2019
End Date
December 5 2019
Last Update
September 6 2019
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