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NCT00540046 · ClinicalTrials.gov registry record · NA
Immediate vs. Delayed Insertion of Copper T 380A IUD After Termination of Pregnancy Over 12-weeks Gestation
A NA study, sponsored by NYU Langone Health.
- Completed
- Registry status
- NA
- Development phase
- 215
- Enrollment target
NCT00540046: Completed NA study, sponsored by NYU Langone Health.
NCT00540046 is a NA study that has completed, run by NYU Langone Health. The registered enrollment target is 215 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00540046, a NA study, has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 215 participants
- Enrollment target
Study 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.
Primary Outcome
Number of participants using Copper T380A IUD 6 months after surgery
Interventions
- DEVICE Copper T 380A IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 215 participants |
| Start Date | 2007-04 |
| Est. Completion | 2010-02 |
| Phase | NA |
What the finished NCT00540046 record still lists
NCT00540046 is an interventional study that assigns participants to a tested intervention. The registered 215 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 1 intervention - of which Copper T 380A IUD is the first listed.
NCT00540046 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00540046 about?
NCT00540046 is a clinical study titled "Immediate vs. Delayed Insertion of Copper T 380A IUD After Termination of Pregnancy Over 12-weeks Gestation". 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.
What is the current status of trial NCT00540046?
This trial is currently completed. It is a NA study. The enrollment target is 215 participants. The study started on 2007-04. Estimated completion is 2010-02.
What interventions are being tested in trial NCT00540046?
The interventions under investigation include: Copper T 380A IUD (DEVICE).
Who is sponsoring clinical trial NCT00540046?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00540046's enrollment target sits among peer trials
215 487th of 2000 higher than 1,514 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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