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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 is a NA study that has completed, run by Boston University. The registered enrollment target is 120 participants.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00621543
The ClinicalTrials.gov registry entry for NCT00621543 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston University, which has 185 total studies on file at ClinicalTrials.gov.
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 reports 0 study locations.
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.
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