CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
Misoprostol +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00613366
NCT00613366N/ACompleted

Effect of Prophylactic Misoprostol Prior to Intrauterine Device Insertion

Oregon Health and Science University·interventional·Posted Feb 13, 2008·Updated Mar 15, 2013

In Brief

A clinical study evaluating Misoprostol and Magnesium Oxide for Contraception. Completed, enrolled 40 participants across 2 sites.

Detailed Summary

The purpose of this study is to see if using misoprostol (a medication that softens the cervix) before placing an intrauterine device for contraception reduces pain in women who have never delivered a baby.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContraception
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 13, 2008
Enrollment StartJun 1, 2007
Primary CompletionApr 1, 2010
Study CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 18.4 years ago

Interventions

Misoprostoldrug

Place 2 tablets between the teeth and cheek and allow to dissolve for 30 minutes.

Magnesium Oxidedietary

Place 2 tablets between the teeth and cheek and allow to dissolve for 30 minutes.