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NCT02144259 · ClinicalTrials.gov registry record · NA

The Impact of Contraception on Postpartum Weight Loss

A NA study, sponsored by University of Pennsylvania.

Completed
Registry status
NA
Development phase
100
Enrollment target

NCT02144259: Completed NA study, sponsored by University of Pennsylvania.

NCT02144259 is a NA study that has completed, run by University of Pennsylvania. The registered enrollment target is 100 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02144259, a NA study, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target

Study Summary

This is a prospective mixed methods study to assess weight changes in women randomized to receive Implanon ® or Depo Provera® (DMPA) immediately postpartum compared to women who choose non-hormonal contraception or no contraception immediately postpartum. After enrollment, subjects return for a visit at 3, 6 and 12 months postpartum to be asked a series of questions, take a pregnancy test, and be weighed. Total length of participation for each subject is 1 year or until pregnancy.

Interventions

  • DRUG DMPA immediately postpartum
  • DRUG Implanon immediately postpartum

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2011-04
Est. Completion 2012-10
Phase NA

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT02144259

The ClinicalTrials.gov registry entry for NCT02144259 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 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 2 interventions - of which DMPA immediately postpartum is the first listed.

NCT02144259 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02144259 about?

NCT02144259 is a clinical study titled "The Impact of Contraception on Postpartum Weight Loss". This is a prospective mixed methods study to assess weight changes in women randomized to receive Implanon ® or Depo Provera® (DMPA) immediately postpartum compared to women who choose non-hormonal contraception or no contraception immediately postpartum. After enrollment, subjects return for a visi...

What is the current status of trial NCT02144259?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2011-04. Estimated completion is 2012-10.

What interventions are being tested in trial NCT02144259?

The interventions under investigation include: DMPA immediately postpartum (DRUG), Implanon immediately postpartum (DRUG).

Who is sponsoring clinical trial NCT02144259?

This trial is sponsored by University of Pennsylvania, which has 1,423 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, the data changelog, or report a data error.