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

NCT00330187 · ClinicalTrials.gov registry record · Phase 2

Combined Pharmaco/Behavior Therapy in Adolescent Smokers

A Phase 2 study, sponsored by Medical University of South Carolina.

Completed
Registry status
Phase 2
Development phase
134
Enrollment target

NCT00330187: Completed Phase 2 study, sponsored by Medical University of South Carolina.

NCT00330187 is a Phase 2 study that has completed, run by Medical University of South Carolina. The registered enrollment target is 134 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00330187, a Phase 2 study, has completed, sponsored by Medical University of South Carolina.

COMPLETED
Registry status
Phase 2
Development phase
134 participants
Enrollment target

Study Summary

In the current proposal, we intend to study the efficacy of bupropion SR with or without combined contingency management (CM) among adolescent cigarette smokers. The proposed study will test not only medication (bupropion SR), but also combination of medication and CM in potentially improving smoking cessation outcomes AND retention of adolescent smokers in the study. Hypothesis to be tested: Bupropion SR treatment will increase abstinence from cigarette smoking (as measured by urine cotinine and continuous abstinence) in adolescent smokers as compared to treatment with placebo only. Hypothesis to be tested: Adolescent smokers treated with combined bupropion SR + contingency management (CM) treatment will have increased retention and increased abstinence rates when compared to bupropion SR alone or CM + placebo treated groups (as measured by decreased drop-out of participants, urine cotinine and continuous abstinence). Hypothesis to be tested: CM will increase the abstinence from cigarette smoking (as measured by urine cotinine and continuous abstinence) in adolescent smokers as compared to treatment with placebo only.

Primary Outcome

Self-reported abstinence for the past 7 days, confirmed by urine cotinine ≤100 ng/mL

Interventions

  • OTHER Placebo
  • BEHAVIORAL Contingency Management
  • DRUG Bupropion SR

Trial Details

FieldValue
Enrollment Target 134 participants
Start Date 2004-03
Est. Completion 2009-07
Phase Phase 2

What the finished NCT00330187 record still lists

NCT00330187 is an interventional study that assigns participants to a tested intervention. The registered 134 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

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

NCT00330187 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00330187 about?

NCT00330187 is a clinical study titled "Combined Pharmaco/Behavior Therapy in Adolescent Smokers". In the current proposal, we intend to study the efficacy of bupropion SR with or without combined contingency management (CM) among adolescent cigarette smokers. The proposed study will test not only medication (bupropion SR), but also combination of medication and CM in potentially improving smokin...

What is the current status of trial NCT00330187?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 134 participants. The study started on 2004-03. Estimated completion is 2009-07.

What interventions are being tested in trial NCT00330187?

The interventions under investigation include: Placebo (OTHER), Contingency Management (BEHAVIORAL), Bupropion SR (DRUG).

Who is sponsoring clinical trial NCT00330187?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00330187's enrollment target sits among peer trials

134 537th of 2000 higher than 1,463 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

  • NCT02469662 · 134 participants · NA

    Clinical Outcomes Study of the Nexel Total Elbow

  • NCT03110822 · 134 participants · Phase 1

    A Phase 1 Study of Ruxolitinib, Steroids and Lenalidomide for Relapsed/Refractory Multiple Myeloma (RRMM) Patients

  • NCT04678648 · 134 participants · Phase 1

    A Trial of RSC-1255 for Treatment of Patients With Advanced Malignancies

  • NCT05264857 · 134 participants · NA

    Decision Aid and Thyroid Nodules Management

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 NCT00330187, the US trial registry maintained by the National Library of Medicine. NCT00330187 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.