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NCT00562276 · ClinicalTrials.gov registry record · Phase 4
Immediate Versus Delayed Intrauterine Device (IUD) Insertion Following First Trimester Suction Aspiration Procedures
A Phase 4 study, sponsored by Oregon Health and Science University.
- Completed
- Registry status
- Phase 4
- Development phase
- 578
- Enrollment target
NCT00562276: Completed Phase 4 study, sponsored by Oregon Health and Science University.
NCT00562276 is a Phase 4 study that has completed, run by Oregon Health and Science University. The registered enrollment target is 578 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (12% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00562276, a Phase 4 study, has completed, sponsored by Oregon Health and Science University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 578 participants
- Enrollment target
Study Summary
The purpose of this multi-center clinical trial is to evaluate the safety and effectiveness of inserting an intrauterine device (IUD) immediately after a suction aspiration procedure compared to inserting the IUD 2-6 weeks after the procedure. This study will also evaluate how satisfied women are with the timing of their IUD placement. Subjects will be able to choose between the Paraguard IUD or the Mirena IUD. The researchers hypothesize that: 1. the expulsion rates measured at 1, 3 and 6 months will be clinically equivalent with immediate insertion compared with delayed insertion, 2. satisfaction and tolerance of side effects will be higher with immediate IUD insertion compared with delayed insertion, and 3. overall IUD use/continuation rates measured at 1, 3 and 6 months will be higher with immediate IUD insertion compared with delayed insertion.
Interventions
- PROCEDURE Immediate IUD insertion
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 578 participants |
| Start Date | 2007-05 |
| Est. Completion | 2009-06 |
| Phase | Phase 4 |
What the finished NCT00562276 record still lists
NCT00562276 is an interventional study that assigns participants to a tested intervention. The registered 578 participants enrollment target is mid-sized for trials with a published cap, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (12% higher).
The record links to 0 conditions, and to 1 intervention - of which Immediate IUD insertion is the first listed.
NCT00562276 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00562276 about?
NCT00562276 is a clinical study titled "Immediate Versus Delayed Intrauterine Device (IUD) Insertion Following First Trimester Suction Aspiration Procedures". The purpose of this multi-center clinical trial is to evaluate the safety and effectiveness of inserting an intrauterine device (IUD) immediately after a suction aspiration procedure compared to inserting the IUD 2-6 weeks after the procedure. This study will also evaluate how satisfied women are wi...
What is the current status of trial NCT00562276?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 578 participants. The study started on 2007-05. Estimated completion is 2009-06.
What interventions are being tested in trial NCT00562276?
The interventions under investigation include: Immediate IUD insertion (PROCEDURE).
Who is sponsoring clinical trial NCT00562276?
This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00562276's enrollment target sits among peer trials
578 149th of 2000 higher than 1,852 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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