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NCT02706340 · ClinicalTrials.gov registry record
Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study
A clinical trial, sponsored by University of Pennsylvania.
- Completed
- Registry status
- 309
- Enrollment target
NCT02706340: Completed study, sponsored by University of Pennsylvania.
NCT02706340 is a clinical trial that has completed, run by University of Pennsylvania. The registered enrollment target is 309 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02706340 has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- 309 participants
- Enrollment target
Study Summary
This is an observational study enrolling women who have had a copper intrauterine device placed immediately after childbirth. The study follows participants for 6 month in order to evaluate the primary outcome of IUD expulsion within 6 months of delivery.
Interventions
- OTHER No intervention - observational study only
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 309 participants |
| Start Date | 2015-04 |
| Est. Completion | 2018-07 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02706340
The ClinicalTrials.gov registry entry for NCT02706340 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 309 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which No intervention - observational study only is the first listed.
NCT02706340 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02706340 about?
NCT02706340 is a clinical study titled "Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study". This is an observational study enrolling women who have had a copper intrauterine device placed immediately after childbirth. The study follows participants for 6 month in order to evaluate the primary outcome of IUD expulsion within 6 months of delivery.
What is the current status of trial NCT02706340?
This trial is currently completed. The enrollment target is 309 participants. The study started on 2015-04. Estimated completion is 2018-07.
What interventions are being tested in trial NCT02706340?
The interventions under investigation include: No intervention - observational study only (OTHER).
Who is sponsoring clinical trial NCT02706340?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
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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, the data changelog, or report a data error.