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

NCT02111798 · ClinicalTrials.gov registry record · Phase 2

Bupropion-Enhanced Contingency Management (CM) for Cocaine Dependence

A Phase 2 study, sponsored by Johns Hopkins University.

Completed
Registry status
Phase 2
Development phase
83
Enrollment target

NCT02111798: Completed Phase 2 study, sponsored by Johns Hopkins University.

NCT02111798 is a Phase 2 study that has completed, run by Johns Hopkins University. The registered enrollment target is 83 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT02111798, a Phase 2 study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
Phase 2
Development phase
83 participants
Enrollment target

Study Summary

This project will examine effects of bupropion extended release (XL) at a dose of 300mg/day for cocaine abstinence among persons receiving methadone for the treatment of opioid use disorder. Participants also earned financial incentives for providing urine samples that tested negative for cocaine. Bupropion was examined for this purpose because of its previously demonstrated efficacy and safety as well as its pharmacological actions at dopamine systems. Participants were randomly assigned to bupropion XL vs. placebo and received different incentive schedules depending on whether they demonstrated abstinence from cocaine early in the study. Outcomes were tracked over a 6-month time frame and the overarching hypothesis was that bupropion (as compared to placebo) would increase the number of urine samples testing negative for cocaine, independent of whether participants demonstrated abstinence from cocaine early in the study.

Primary Outcome

Comparison of the number of thrice-weekly urine tests submitted during weeks study 7-30 negative for cocaine for persons randomly assigned to receive placebo or bupropion XL during weeks 7-30; excused samples are omitted and missing samples are treated as positive.

Interventions

  • DRUG Placebo
  • BEHAVIORAL Relapse Prevention
  • DRUG Bupropion XL
  • BEHAVIORAL Abstinence Initiation

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2014-07
Est. Completion 2021-01
Phase Phase 2
Johns Hopkins University

1,448 total trials

What the finished NCT02111798 record still lists

NCT02111798 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02111798 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02111798 about?

NCT02111798 is a clinical study titled "Bupropion-Enhanced Contingency Management (CM) for Cocaine Dependence". This project will examine effects of bupropion extended release (XL) at a dose of 300mg/day for cocaine abstinence among persons receiving methadone for the treatment of opioid use disorder. Participants also earned financial incentives for providing urine samples that tested negative for cocaine. B...

What is the current status of trial NCT02111798?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 83 participants. The study started on 2014-07. Estimated completion is 2021-01.

What interventions are being tested in trial NCT02111798?

The interventions under investigation include: Placebo (DRUG), Relapse Prevention (BEHAVIORAL), Bupropion XL (DRUG), Abstinence Initiation (BEHAVIORAL).

Who is sponsoring clinical trial NCT02111798?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02111798's enrollment target sits among peer trials

83 828th of 2000 higher than 1,171 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02974647 · 83 participants · Phase 2

    Study of Ruxolitinib in Relapsed or Refractory T or NK Cell Lymphoma

  • NCT03919292 · 83 participants · Phase 1

    Neratinib + Valproate in Advanced Solid Tumors, w/Expansion Cohort in Ras-Mutated Ca

  • NCT04626674 · 83 participants · Phase 1

    A Gene Transfer Therapy Study to Evaluate the Safety of and Expression From Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)

  • NCT05277168 · 83 participants · Phase 1

    A Trial TO Evaluate THE Safety, Tolerability, Pharmacokinetics, AND Efficacy OF Shr-a1904 IN Subjects With Advanced Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02111798, the US trial registry maintained by the National Library of Medicine. NCT02111798 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.