Clinical Trials Directory

Trials / Completed

CompletedNCT00540046

Immediate vs. Delayed Insertion of Copper T 380A IUD After Termination of Pregnancy Over 12-weeks Gestation

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
215 (actual)
Sponsor
NYU Langone Health · Academic / Other
Sex
Female
Age
16 Years
Healthy volunteers
Accepted

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.

Detailed description

Patients presenting to ParkMed Women's Clinic and the Reproductive Choice clinic at Bellevue Hospital for second trimester termination will be offered participation in this study. They will be randomized to either delayed or immediate Copper T 380A IUD insertion. The subjects will be seen at a 6 month follow-up visit and Copper T 380A IUD placement will be verified by physical exam. At this 6 month follow-up visit, subjects will fill out a satisfaction questionnaire.

Conditions

Interventions

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

Timeline

Start date
2007-04-01
Primary completion
2010-02-01
Completion
2010-02-01
First posted
2007-10-05
Last updated
2015-02-09
Results posted
2015-01-13

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00540046. Inclusion in this directory is not an endorsement.