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NCT01666912 · ClinicalTrials.gov registry record · Phase 4
Postpartum Etonogestrel Implant for Adolescents
A Phase 4 study of Contraception and Postpartum, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- Phase 4
- Development phase
- 96
- Enrollment target
- 1
- Study location
NCT01666912 is a Phase 4 study of Contraception and Postpartum that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 96 participants, below the 453-participant average among 72 other Contraception trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01666912, a Phase 4 study of Contraception and Postpartum, has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 96 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a prospective study comparing two groups of 48 adolescent women each. The intervention group will receive a contraceptive implant postpartum, prior to discharge from the hospital. The control group will receive a contraceptive implant at the usual 6 week postpartum clinic visit. During prenatal care, participants will be consented and screened for enrollment. After delivery, these women will be assessed and consented for enrollment into the study. Women who consent for enrollment will be randomized. Women will be followed up at 3 months, 6 months, 9 months, and 1 year after contraceptive implant insertion. At each follow up, women will be assessed for continuation of and satisfaction with this method of contraception.
Conditions Studied
Interventions
- DRUG Contraceptive implant
Study Locations (1)
North Carolina
- University of North Carolina Hospitals - Chapel Hill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 96 participants |
| Start Date | 2012-08 |
| Est. Completion | 2015-04 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01666912
The ClinicalTrials.gov registry entry for NCT01666912 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 96 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 453-participant average among 72 other Contraception trials with a reported enrollment target (79% 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 3 conditions, with Contraception appearing as the primary indexed condition, and to 1 intervention - of which Contraceptive implant is the first listed.
NCT01666912 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT01666912 about?
NCT01666912 is a clinical study titled "Postpartum Etonogestrel Implant for Adolescents". This is a prospective study comparing two groups of 48 adolescent women each. The intervention group will receive a contraceptive implant postpartum, prior to discharge from the hospital. The control group will receive a contraceptive implant at the usual 6 week postpartum clinic visit. During prena...
What is the current status of trial NCT01666912?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 96 participants. The study started on 2012-08. Estimated completion is 2015-04.
What conditions does trial NCT01666912 study?
This clinical trial studies the following conditions: Contraception, Postpartum, Adolescence.
What interventions are being tested in trial NCT01666912?
The interventions under investigation include: Contraceptive implant (DRUG).
Who is sponsoring clinical trial NCT01666912?
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 NCT01666912 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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