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NCT00997932 · ClinicalTrials.gov registry record · Phase 4
A Pilot Study of Early Postpartum Intrauterine Contraception
A Phase 4 study of Unplanned Pregnancy, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- Phase 4
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT00997932 is a Phase 4 study of Unplanned Pregnancy that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 40 participants, below the 198-participant average among 3 other Unplanned Pregnancy trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00997932, a Phase 4 study of Unplanned Pregnancy, has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a prospective clinical trial of ultrasound guided intrauterine contraception insertion 10 minutes - 48 hours after vaginal delivery of single infant. A six month follow-up will entail three follow-up visits; 4-6 weeks, 3 months, and 6 months. The objective of this study is to measure intrauterine device (IUD) expulsion and the feasibility of conducting a future clinical trial to evaluate placement of the levonorgestrel-releasing intrauterine contraceptive 10 minutes - 48 hours postpartum.
Conditions Studied
Interventions
- DRUG Levonorgestrel-Releasing Intrauterine Contraceptive System (LNG-IUS), 52 Mg, 5 Year Duration
Study Locations (1)
North Carolina
- University of North Carolina at Chapel Hill - Chapel Hill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2009-06 |
| Est. Completion | 2012-11 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00997932
The ClinicalTrials.gov registry entry for NCT00997932 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 198-participant average among 3 other Unplanned Pregnancy trials with a reported enrollment target (80% lower). The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Unplanned Pregnancy appearing as the primary indexed condition, and to 1 intervention - of which Levonorgestrel-Releasing Intrauterine Contraceptive System (LNG-IUS), 52 Mg, 5 Year Duration is the first listed.
NCT00997932 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT00997932 about?
NCT00997932 is a clinical study titled "A Pilot Study of Early Postpartum Intrauterine Contraception". This is a prospective clinical trial of ultrasound guided intrauterine contraception insertion 10 minutes - 48 hours after vaginal delivery of single infant. A six month follow-up will entail three follow-up visits; 4-6 weeks, 3 months, and 6 months. The objective of this study is to measure intrau...
What is the current status of trial NCT00997932?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2009-06. Estimated completion is 2012-11.
What conditions does trial NCT00997932 study?
This clinical trial studies the following conditions: Unplanned Pregnancy.
What interventions are being tested in trial NCT00997932?
The interventions under investigation include: Levonorgestrel-Releasing Intrauterine Contraceptive System (LNG-IUS), 52 Mg, 5 Year Duration (DRUG).
Who is sponsoring clinical trial NCT00997932?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00997932 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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