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NCT02173886 · ClinicalTrials.gov registry record · Phase 4

A Comparison of Sustained and Extended Release Bupropion Following Bariatric Surgery

A Phase 4 study, sponsored by North Dakota State University.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target

NCT02173886 is a Phase 4 study that has completed, run by North Dakota State University. The registered enrollment target is 20 participants.

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The verdict

NCT02173886, a Phase 4 study, has completed, sponsored by North Dakota State University.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target

Study Summary

This study is being conducted to evaluate how the body absorbs and processes the sustained release (SR) and extended release (XL) medication bupropion (Wellbutrin®). Subject who are 1-3 years post gastric bypass surgery will be invited to participate. Non-surgical controls will also be enrolled based on a matching criteria to post gastric bypass subjects. Participants will be asked to complete two 12-hour study days approximately 11 days apart.

Interventions

  • DRUG Bupropion SR and XL

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2014-06
Est. Completion 2015-02
Phase Phase 4

Sponsor

North Dakota State University

16 total trials

What the Registry Record Tells You About NCT02173886

The ClinicalTrials.gov registry entry for NCT02173886 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is North Dakota State University, which has 16 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bupropion SR and XL is the first listed.

NCT02173886 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02173886 about?

NCT02173886 is a clinical study titled "A Comparison of Sustained and Extended Release Bupropion Following Bariatric Surgery". This study is being conducted to evaluate how the body absorbs and processes the sustained release (SR) and extended release (XL) medication bupropion (Wellbutrin®). Subject who are 1-3 years post gastric bypass surgery will be invited to participate. Non-surgical controls will also be enrolled base...

What is the current status of trial NCT02173886?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2014-06. Estimated completion is 2015-02.

What interventions are being tested in trial NCT02173886?

The interventions under investigation include: Bupropion SR and XL (DRUG).

Who is sponsoring clinical trial NCT02173886?

This trial is sponsored by North Dakota State University, which has 16 total clinical trials registered on ClinicalTrials.gov.

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

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.