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NCT02657148 · ClinicalTrials.gov registry record
Immediate Postpartum Nexplanon Placement in Opioid Dependent Women
A clinical trial, sponsored by University of Pittsburgh.
- Completed
- Registry status
- 200
- Enrollment target
NCT02657148: Completed study, sponsored by University of Pittsburgh.
NCT02657148 is a clinical trial that has completed, run by University of Pittsburgh. The registered enrollment target is 200 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02657148 has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- 200 participants
- Enrollment target
Study Summary
The investigators have designed a single site, Phase IV open label, prospective observational clinical trial to compare the effect of immediate postpartum Nexplanon placement (IPP) versus standard postpartum contraceptive care (control) on consistent contraceptive use and rapid repeat pregnancy at 12 months postpartum in 200 opioid dependent (OD) women.
Primary Outcome
Number of participants who use highly effective contraception (all hormonal methods or the copper T380 IUD) for ≥ 80% of the first postpartum year
Interventions
- DRUG Nexplanon (etonogestrel contraceptive implant)
- DRUG Standard postpartum contraceptive care
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2016-05 |
| Est. Completion | 2018-08 |
What the finished NCT02657148 record still lists
NCT02657148 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 2 interventions - of which Nexplanon (etonogestrel contraceptive implant) is the first listed.
NCT02657148 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02657148 about?
NCT02657148 is a clinical study titled "Immediate Postpartum Nexplanon Placement in Opioid Dependent Women". The investigators have designed a single site, Phase IV open label, prospective observational clinical trial to compare the effect of immediate postpartum Nexplanon placement (IPP) versus standard postpartum contraceptive care (control) on consistent contraceptive use and rapid repeat pregnancy at 1...
What is the current status of trial NCT02657148?
This trial is currently completed. The enrollment target is 200 participants. The study started on 2016-05. Estimated completion is 2018-08.
What interventions are being tested in trial NCT02657148?
The interventions under investigation include: Nexplanon (etonogestrel contraceptive implant) (DRUG), Standard postpartum contraceptive care (DRUG).
Who is sponsoring clinical trial NCT02657148?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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