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
| Type | Name | Description |
|---|---|---|
| DEVICE | Copper T 380A IUD | Copper 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.