Overview
Comparison Between 2 Doses of Misoprostol Before Intrauterine Device
Status:
Completed
Completed
Trial end date:
2017-01-01
2017-01-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of the investigators' study was to evaluate whether misoprostol will improve pain scores .Phase:
Phase 2/Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Assiut UniversityTreatments:
Misoprostol
Criteria
Inclusion Criteria:- • Women not taken analgesics or anxiolytics in the 24 hours prior insertion
- Women who will accept to participate in the study
Exclusion Criteria:
- Any contraindication to IUD placement