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NCT01350011 · ClinicalTrials.gov registry record · Phase 3

Tobacco Intervention in Buprenorphine Treatment

A Phase 3 study, sponsored by University of California, San Francisco.

Completed
Registry status
Phase 3
Development phase
175
Enrollment target

NCT01350011: Completed Phase 3 study, sponsored by University of California, San Francisco.

NCT01350011 is a Phase 3 study that has completed, run by University of California, San Francisco. The registered enrollment target is 175 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01350011, a Phase 3 study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
Phase 3
Development phase
175 participants
Enrollment target

Study Summary

Drug addiction treatment patients, including those in treatment for opioid dependence, have a high rate of tobacco dependence, especially cigarette smoking. The proposed study evaluates an Innovative System (IS) for the treatment of tobacco dependence in one group of opioid treatment patients, those in buprenorphine maintenance. The specific aims of the study are to test the efficacy and the cost effectiveness of the IS. A secondary aim is obtain preliminary data about differences in use of non-nicotinic drugs between participants who achieve abstinence from cigarettes during the study, and those who do not.

Primary Outcome

Smoking status is defined as "no cigarettes for the past 7 days."

Interventions

  • BEHAVIORAL Innovative System
  • BEHAVIORAL Standard Treatment Control (STC)

Trial Details

FieldValue
Enrollment Target 175 participants
Start Date 2011-04-01
Est. Completion 2016-12-01
Phase Phase 3

What the finished NCT01350011 record still lists

NCT01350011 is an interventional study that assigns participants to a tested intervention. The registered 175 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 2 interventions - of which Innovative System is the first listed.

NCT01350011 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01350011 about?

NCT01350011 is a clinical study titled "Tobacco Intervention in Buprenorphine Treatment". Drug addiction treatment patients, including those in treatment for opioid dependence, have a high rate of tobacco dependence, especially cigarette smoking. The proposed study evaluates an Innovative System (IS) for the treatment of tobacco dependence in one group of opioid treatment patients, those...

What is the current status of trial NCT01350011?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 175 participants. The study started on 2011-04-01. Estimated completion is 2016-12-01.

What interventions are being tested in trial NCT01350011?

The interventions under investigation include: Innovative System (BEHAVIORAL), Standard Treatment Control (STC) (BEHAVIORAL).

Who is sponsoring clinical trial NCT01350011?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01350011's enrollment target sits among peer trials

175 1440th of 2000 higher than 559 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01350011, the US trial registry maintained by the National Library of Medicine. NCT01350011 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.