CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 215 enrolled
Drug / intervention
Copper T 380A 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/NCT00540046
NCT00540046N/ACompleted
CompareCT.gov

Immediate vs. Delayed Post-abortal Copper T 380A IUD Insertion in Cases Over 12 Weeks of Gestation

NYU Langone Health·interventional·Posted Oct 5, 2007·Updated Feb 9, 2015

In Brief

A clinical study evaluating Copper T 380A IUD for Contraception Behavior. Completed, enrolled 215 participants across 2 sites.

Detailed Summary

The purpose of this study is to compare delayed vs. immediate insertion of the Copper T 380 IUD after termination of pregnancy after 12 weeks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContraception Behavior
CountriesUnited States
CollaboratorsIcahn School of Medicine at Mount Sinai

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 5, 2007
Enrollment StartApr 1, 2007
Primary CompletionFeb 1, 2010
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 18.7 years ago

Interventions

Copper T 380A IUDdevice

Copper T 380A IUD will be placed at the 2-4 week post-operative visit.