CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 404 enrolled
Drug / intervention
IUDdevice
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/NCT03462758
NCT03462758N/ACompleted
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Early vs. Interval Postpartum IUD Insertion: A Multi-site Randomized Controlled Trial

University of California, San Diego·interventional·Posted Mar 13, 2018·Updated Apr 13, 2023

In Brief

A clinical study evaluating IUD for Contraception. Completed, enrolled 404 participants across 4 sites.

Detailed Summary

Intrauterine devices (IUDs) are historically placed at a six-week postpartum visit for women who desire intrauterine contraception after delivery. A two-week postpartum visit could be a convenient time for women to receive contraception, including IUDs. Offering women IUDs at two-weeks postpartum may decrease the risk of undesired pregnancy and rapid repeat pregnancy. This study will compare IUD insertion at two different times after delivery: two-weeks and six-weeks postpartum. This will allow researchers to assess whether the timing of IUD placement affects whether an IUD is expelled, or pushed out of it's ideal location.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContraception
CountriesUnited States
CollaboratorsUniversity of New Mexico, United States Naval Medical Center, San Diego, University of Illinois at Chicago, University of Chicago

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedMar 13, 2018
Enrollment StartMar 20, 2018
Primary CompletionAug 14, 2022
Study CompletionDec 31, 2022
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 8.3 years ago

Interventions

IUDdevice

Postpartum IUD placement