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NCT02773212 · ClinicalTrials.gov registry record · Phase 2

Targeting Anhedonia in Cocaine Use Disorder

A Phase 2 study, sponsored by University of Illinois at Chicago.

Completed
Registry status
Phase 2
Development phase
57
Enrollment target

NCT02773212: Completed Phase 2 study, sponsored by University of Illinois at Chicago.

NCT02773212 is a Phase 2 study that has completed, run by University of Illinois at Chicago. The registered enrollment target is 57 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02773212, a Phase 2 study, has completed, sponsored by University of Illinois at Chicago.

COMPLETED
Registry status
Phase 2
Development phase
57 participants
Enrollment target

Study Summary

The purpose of this study is to examine anhedonia as a potential moderator of treatment outcomes for Cocaine Use Disorder (CUD). Specifically, this study will investigate how anhedonia affects outcomes in contingency management (CM) treatment for CUD and whether anhedonia mediates the effects of adjunctive treatment with a dopaminergic (DAergic) drug, d-amphetamine, on outcomes in CM for CUD, as well as investigate the contribution of anhedonia to overall CUD severity.

Primary Outcome

Subjects will complete a urine drug screen each visit. Achievement of cocaine abstinence will be defined as two consecutive weeks of cocaine-negative urine samples.

Interventions

  • BEHAVIORAL Contingency management
  • DRUG d-amphetamine
  • DRUG Placebo (for d-amphetamine)

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2017-02-01
Est. Completion 2022-04-04
Phase Phase 2
University of Illinois at Chicago

430 total trials

What the finished NCT02773212 record still lists

NCT02773212 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 57 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 3 interventions - of which Contingency management is the first listed.

NCT02773212 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02773212 about?

NCT02773212 is a clinical study titled "Targeting Anhedonia in Cocaine Use Disorder". The purpose of this study is to examine anhedonia as a potential moderator of treatment outcomes for Cocaine Use Disorder (CUD). Specifically, this study will investigate how anhedonia affects outcomes in contingency management (CM) treatment for CUD and whether anhedonia mediates the effects of adj...

What is the current status of trial NCT02773212?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 57 participants. The study started on 2017-02-01. Estimated completion is 2022-04-04.

What interventions are being tested in trial NCT02773212?

The interventions under investigation include: Contingency management (BEHAVIORAL), d-amphetamine (DRUG), Placebo (for d-amphetamine) (DRUG).

Who is sponsoring clinical trial NCT02773212?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02773212's enrollment target sits among peer trials

57 1141st of 2000 higher than 855 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

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Source: ClinicalTrials.gov NCT02773212, the US trial registry maintained by the National Library of Medicine. NCT02773212 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.