Comparison Between 2 Doses of Misoprostol Before Intrauterine Device

NCT02901561 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 212

Last updated 2017-03-14

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02901561 on ClinicalTrials.gov