Comparison Between 2 Doses of Misoprostol Before Intrauterine Device
NCT02901561 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 212
Last updated 2017-03-14
Summary
The purpose of the investigators' study was to evaluate whether misoprostol will improve pain scores .
Conditions
- Pain Relief
Interventions
- DRUG
-
misoprostol 200
- DRUG
-
misoprostol 400
Sponsors & Collaborators
-
Assiut University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 49 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-09-30
- Primary Completion
- 2016-12-31
- Completion
- 2017-01-31
Countries
- Egypt
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