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NCT00621543 · ClinicalTrials.gov registry record · NA
Insertion of an Intrauterine Device (IUD) After Medical Abortion
A NA study, sponsored by Boston University.
- Completed
- Registry status
- NA
- Development phase
- 120
- Enrollment target
NCT00621543: Completed NA study, sponsored by Boston University.
NCT00621543 is a NA study that has completed, run by Boston University. The registered enrollment target is 120 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00621543, a NA study, has completed, sponsored by Boston University.
- COMPLETED
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the expulsion and continuation rate of an intruterine device (IUD) placed immediately after medical abortion. Our hypothesis is that immediate-placement of an IUD after completed medical abortion will have a similar expulsion and continuation rate to traditional placement (4-6 weeks after pregnancy).
Interventions
- DEVICE IUD insertion [Copper T-380A or Levonorgestrel (intrauterine system) IUS]
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2006-03 |
| Est. Completion | 2008-09 |
| Phase | NA |
What the finished NCT00621543 record still lists
NCT00621543 is an interventional study that assigns participants to a tested intervention. The registered 120 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 (91% lower).
The record links to 0 conditions, and to 1 intervention - of which IUD insertion [Copper T-380A or Levonorgestrel (intrauterine system) IUS] is the first listed.
NCT00621543 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00621543 about?
NCT00621543 is a clinical study titled "Insertion of an Intrauterine Device (IUD) After Medical Abortion". The purpose of this study is to determine the expulsion and continuation rate of an intruterine device (IUD) placed immediately after medical abortion. Our hypothesis is that immediate-placement of an IUD after completed medical abortion will have a similar expulsion and continuation rate to tradit...
What is the current status of trial NCT00621543?
This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2006-03. Estimated completion is 2008-09.
What interventions are being tested in trial NCT00621543?
The interventions under investigation include: IUD insertion [Copper T-380A or Levonorgestrel (intrauterine system) IUS] (DEVICE).
Who is sponsoring clinical trial NCT00621543?
This trial is sponsored by Boston University, which has 185 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00621543's enrollment target sits among peer trials
120 762nd of 2000 higher than 1,198 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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