Viewing Study NCT00749658


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Study NCT ID: NCT00749658
Status: COMPLETED
Last Update Posted: 2020-11-23
First Post: 2008-09-05
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Human Laboratory Study of Varenicline and Bupropion for Nicotine Dependence
Sponsor: University of Minnesota
Organization:

Study Overview

Official Title: Human Laboratory Study of Varenicline and Bupropion for Nicotine Dependence
Status: COMPLETED
Status Verified Date: 2020-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ChanBan
Brief Summary: The objective of this proposal is to elucidate effects of bupropion SR + varenicline on smoking-cessation related processes in early abstinence using a human laboratory model. A within-subjects design will be used to assess the additive effects of bupropion and varenicline in 48 treatment seeking smokers \[bupropion SR (300 mg/day)+placebo, varenicline (2 mg/day+placebo, and bupropion SR (300 mg/day)+varenicline (2 mg/day)\]. Outcomes include withdrawal and craving, cognition, stress tolerance, anxiety, the reinforcing effects of smoking, and smoking topography.

Hypotheses: We hypothesize that greatest treatment effects will be observed in the bupropion SR+varenicline group followed by varenicline+placebo and bupropion SR+placebo groups.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
K01DA019446 NIH None https://reporter.nih.gov/quic… View
DPMC OTHER NIDA View