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NCT00108537 · ClinicalTrials.gov registry record · Phase 3
Non-Nicotine Agents for Smoking Cessation
A Phase 3 study of Tobacco Use Disorder, sponsored by US Department of Veterans Affairs.
- Completed
- Registry status
- Phase 3
- Development phase
- 1
- Study location
NCT00108537: Completed Phase 3 study of Tobacco Use Disorder, sponsored by US Department of Veterans Affairs.
NCT00108537 is a Phase 3 study of Tobacco Use Disorder that has completed, run by US Department of Veterans Affairs. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00108537, a Phase 3 study of Tobacco Use Disorder, has completed, sponsored by US Department of Veterans Affairs.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 1
- Study location
Study Summary
The primary objective of this study is to determine which is the better approach to smoking cessation in veterans: bupropion combined with transdermal nicotine or high dose nicotine replacement therapy (NRT) using transdermal nicotine combined with nicotine inhaler.
Conditions Studied
Interventions
- DRUG bupropion and transdermal patch
- DRUG transdermal patch and nicotine inhaler
Study Locations (1)
Colorado
- Denver VA Medical Center - Denver
Trial Details
| Field | Value |
|---|---|
| Start Date | 2003-10 |
| Est. Completion | 2005-09 |
| Phase | Phase 3 |
What the finished NCT00108537 record still lists
NCT00108537 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.
The record links to 1 condition, with Tobacco Use Disorder appearing as the primary indexed condition, and to 2 interventions - of which bupropion and transdermal patch is the first listed.
NCT00108537 reports a single indexed study location in Colorado.
Frequently Asked Questions
What is clinical trial NCT00108537 about?
NCT00108537 is a clinical study titled "Non-Nicotine Agents for Smoking Cessation". The primary objective of this study is to determine which is the better approach to smoking cessation in veterans: bupropion combined with transdermal nicotine or high dose nicotine replacement therapy (NRT) using transdermal nicotine combined with nicotine inhaler.
What is the current status of trial NCT00108537?
This trial is currently completed. It is a Phase 3 study. The study started on 2003-10. Estimated completion is 2005-09.
What conditions does trial NCT00108537 study?
This clinical trial studies the following conditions: Tobacco Use Disorder.
What interventions are being tested in trial NCT00108537?
The interventions under investigation include: bupropion and transdermal patch (DRUG), transdermal patch and nicotine inhaler (DRUG).
Who is sponsoring clinical trial NCT00108537?
This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00108537 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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