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NCT01062932 · ClinicalTrials.gov registry record · Phase 1
Investigation of Cycloserine as a Smoking Cessation Treatment
A Phase 1 study of Nicotine Addiction, sponsored by Baylor College of Medicine.
- Completed
- Registry status
- Phase 1
- Development phase
- 34
- Enrollment target
- 1
- Study location
NCT01062932: Completed Phase 1 study of Nicotine Addiction, sponsored by Baylor College of Medicine.
NCT01062932 is a Phase 1 study of Nicotine Addiction that has completed, run by Baylor College of Medicine. The registered enrollment target is 34 participants, below the 721-participant average among 10 other Nicotine Addiction trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01062932, a Phase 1 study of Nicotine Addiction, has completed, sponsored by Baylor College of Medicine.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 34 participants
- Enrollment target
- 1
- Study location
Study Summary
Psychosocial treatments for drug abuse benefit some patients (Rawson et al 2004), but there is an urgent need for new treatment approaches that can improve treatment outcomes. One new approach involves facilitation of extinction of conditioned responses through the use of d-cycloserine, a partial agonist at the NMDA glycine site. This approach has proved useful for the treatment of several anxiety disorders. For example, treatment with d-cycloserine enhanced the efficacy of behavioral treatments for acrophobia (Ressler et al 2004) and social phobia (Hofmann et al 2006) by enhancing extinction of conditioned fear responses. This suggests that d-cycloserine has potential to enhance the efficacy of behavioral treatments for drug dependence by enhancing extinction of conditioned responses to drug cues. In this Phase I Cutting-Edge Basic Research Awards (CEBRA) application we propose a proof-of-concept study to examine effects of treatment with d-cycloserine for facilitating extinction of craving provoked by exposure to cigarette smoking cues. The benefits of this treatment approach together with cognitive behavioral treatment for reducing cigarette smoking will then be determined. Smoking cues will be presented using an established virtual reality simulator(Bordnick et al 2004; Bordnick et al 2005a)
Primary Outcome
The study will evaluate the effects of treatment with d-cycloserine (50mg administered prior to each exposure treatment) or placebo (n=20 per cell), on the efficacy exposure therapy using a virtual reality cue for smoking cessation when combined with cognitive behavioral therapy (CBT). Craving ratings will be assessed using standard questionnaires, which will be completed prior to and following virtual reality cue exposure. Smoking cessation and cocaine use will be assessed at three follow-up vi
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Cycloserine
Study Locations (1)
Texas
- Michael E. DeBakey VA Medical Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2009-05 |
| Est. Completion | 2010-09 |
| Phase | Phase 1 |
What the finished NCT01062932 record still lists
NCT01062932 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 721-participant average among 10 other Nicotine Addiction trials with a reported enrollment target (95% lower).
The record links to 1 condition, with Nicotine Addiction appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT01062932 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT01062932 about?
NCT01062932 is a clinical study titled "Investigation of Cycloserine as a Smoking Cessation Treatment". Psychosocial treatments for drug abuse benefit some patients (Rawson et al 2004), but there is an urgent need for new treatment approaches that can improve treatment outcomes. One new approach involves facilitation of extinction of conditioned responses through the use of d-cycloserine, a partial ag...
What is the current status of trial NCT01062932?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2009-05. Estimated completion is 2010-09.
What conditions does trial NCT01062932 study?
This clinical trial studies the following conditions: Nicotine Addiction.
What interventions are being tested in trial NCT01062932?
The interventions under investigation include: Placebo (DRUG), Cycloserine (DRUG).
Who is sponsoring clinical trial NCT01062932?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01062932 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Nicotine Addiction
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01062932's enrollment target sits among peer trials
34 11th of 10 the lowest of 10 other Nicotine Addiction trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Nicotine Addiction 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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