Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01864629 · ClinicalTrials.gov registry record · NA

Optimizing Postpartum Contraception in Women With Preterm Births

A NA study, sponsored by University of Utah.

Completed
Registry status
NA
Development phase
134
Enrollment target

NCT01864629 is a NA study that has completed, run by University of Utah. The registered enrollment target is 134 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01864629, a NA study, has completed, sponsored by University of Utah.

COMPLETED
Registry status
NA
Development phase
134 participants
Enrollment target

Study Summary

The purpose of this study is to examine the effectiveness of focused family planning counseling on the uptake and continuation of highly effective contraceptive methods (defined as the intrauterine device, implant, and both male and female sterilization methods including vasectomy, tubal ligation and Essure) during the postpartum period in women who have recently experienced a preterm delivery. The investigators hypothesize that women with a recent preterm birth (PTB) will be more likely to initiate and continue using a highly effective method of contraception when provided with focused family planning counseling.

Interventions

  • BEHAVIORAL Focused contraception counseling

Trial Details

FieldValue
Enrollment Target 134 participants
Start Date 2013-04
Est. Completion 2016-01
Phase NA

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT01864629

The ClinicalTrials.gov registry entry for NCT01864629 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 134 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Focused contraception counseling is the first listed.

NCT01864629 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01864629 about?

NCT01864629 is a clinical study titled "Optimizing Postpartum Contraception in Women With Preterm Births". The purpose of this study is to examine the effectiveness of focused family planning counseling on the uptake and continuation of highly effective contraceptive methods (defined as the intrauterine device, implant, and both male and female sterilization methods including vasectomy, tubal ligation an...

What is the current status of trial NCT01864629?

This trial is currently completed. It is a NA study. The enrollment target is 134 participants. The study started on 2013-04. Estimated completion is 2016-01.

What interventions are being tested in trial NCT01864629?

The interventions under investigation include: Focused contraception counseling (BEHAVIORAL).

Who is sponsoring clinical trial NCT01864629?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.