Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01598662 · ClinicalTrials.gov registry record · NA
Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement
A NA study, sponsored by University of Louisville.
- Terminated
- Registry status
- NA
- Development phase
- 32
- Enrollment target
NCT01598662 is a NA study that was terminated before completion, run by University of Louisville. The registered enrollment target is 32 participants.
The verdict
NCT01598662, a NA study, was terminated before completion, sponsored by University of Louisville.
- TERMINATED
- Registry status
- NA
- Development phase
- 32 participants
- Enrollment target
Study Summary
This is randomized controlled trial designed for pregnant women who deliver vaginally at the University of Louisville Hospital and desire to have an intrauterine device (IUD) inserted for postpartum contraception. After informed consent is obtained, eligible study participants will be randomized to receive the Mirena® IUD at the 6 week postpartum visit or within 10 minutes of delivery of the placenta following a normal vaginal delivery. The investigators seek to determine the expulsion rate and complication rate in subjects with IUD immediately after placental delivery compared to insertion at six weeks postpartum or later. The investigators hypothesize that immediate placement safe and has an acceptably low expulsion rate to merit earlier placement in the indigent population.
Interventions
- DEVICE Mirena (levonorgestrel-releasing intrauterine system)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2009-07 |
| Est. Completion | 2012-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01598662
The ClinicalTrials.gov registry entry for NCT01598662 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Mirena (levonorgestrel-releasing intrauterine system) is the first listed.
NCT01598662 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01598662 about?
NCT01598662 is a clinical study titled "Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement". This is randomized controlled trial designed for pregnant women who deliver vaginally at the University of Louisville Hospital and desire to have an intrauterine device (IUD) inserted for postpartum contraception. After informed consent is obtained, eligible study participants will be randomized to ...
What is the current status of trial NCT01598662?
This trial is currently terminated. It is a NA study. The enrollment target is 32 participants. The study started on 2009-07. Estimated completion is 2012-07.
What interventions are being tested in trial NCT01598662?
The interventions under investigation include: Mirena (levonorgestrel-releasing intrauterine system) (DEVICE).
Who is sponsoring clinical trial NCT01598662?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.