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Bupropion for Hospitalized Smokers With Acute Cardiovascular Disease

Primary Purpose

Smoking, Myocardial Infarction, Unstable Angina

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
bupropion SR (sustained-release)
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Smoking focused on measuring Smoking cessation, Bupropion SR, Hospital intervention, Myocardial infarction, Unstable angina

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: >18 years old, had smoked >1 cigarette in the past month, were admitted to the hospital with a diagnosis of acute cardiovascular disease (see below) had an expected hospital stay of >24 hours. Eligible admission diagnoses included (1) acute ischemic coronary heart disease (MI or unstable angina), (2) coronary artery bypass graft surgery, or (3) other cardiovascular conditions (congestive heart failure, cardiac arrhythmia, valvular heart disease, or atherosclerotic disease of the aorta, carotid, renal or peripheral arteries) in subjects with documented coronary artery disease. Exclusion Criteria: not willing to consider smoking cessation after discharge, a contraindication to bupropion (seizure disorder, monoamine oxidase inhibitor use, history of anorexia nervosa or bulimia, bupropion allergy) a condition that increased the risk of seizure (e.g., serious head trauma with loss of consciousness uncontrolled hypertension (BP >160/100) in hospital heavy alcohol use (>3 drinks/day) or binge drinking (>6 drinks for males or >5 drinks for females) at least monthly renal insufficiency (serum creatinine >2.0 mg/dl), severe hepatic disease severe depression or severe cognitive impairment or psychosis life expectancy of <12 months, illegal drug use in the past 6 months bupropion use in the past month non-English speaking no telephone residence outside a defined geographic area.

Sites / Locations

  • Massachusetts General Hospital

Outcomes

Primary Outcome Measures

Cotinine-validated 7-day point prevalence tobacco abstinence at 1 year follow-up
Cotinine-validated 7-day point prevalence tobacco abstinence at 3 month follow-up (end of treatment)

Secondary Outcome Measures

Combined fatal and nonfatal cardiovascular events at 3 month follow-up (end of treatment)
Combined fatal and nonfatal cardiovascular events at 1 year follow-up
Cardiovascular mortality at 1 year follow-up
Blood pressure elevation (SBP>160 or DBP>100) during treatment with study drug

Full Information

First Posted
September 13, 2005
Last Updated
September 13, 2005
Sponsor
Massachusetts General Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00181818
Brief Title
Bupropion for Hospitalized Smokers With Acute Cardiovascular Disease
Official Title
Safety and Efficacy of Sustained-Release (SR) Bupropion for Smokers Hospitalized Smokers With Acute Coronary Heart Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
October 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Massachusetts General Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), GlaxoSmithKline

4. Oversight

5. Study Description

Brief Summary
The purpose of the study is to test the efficacy and safety of bupropion SR for smokers hospitalized with acute cardiovascular disease.
Detailed Description
Each year, over 2 million Americans are hospitalized with a myocardial infarction (MI) or unstable angina pectoris, two acute and potentially fatal manifestations of coronary heart disease (CHD). Smoking cessation is highly cost-effective and universally recommended for the approximately 20% of these patients who smoke. Hospitalization for acute CHD is an excellent time to initiate smoking cessation because hospitalization requires temporary tobacco abstinence at the same time that illness increases smokers' motivation to quit. Unfortunately, at least 40% of smokers fail to quit even with optimal cognitive-behavioral counseling interventions that begin in the hospital and continue after discharge. More powerful intervention strategies are needed. Adding pharmacotherapy to behavioral counseling, which is standard practice in outpatients, has not been tested in this setting because of concern about the safety of nicotine replacement after MI. Sustained release (SR) bupropion (Zyban, Wellbutrin SR) is a non-nicotine antidepressant drug that has recently proved to be effective for smoking cessation. It appears to be safe in cardiac patients and may have the additional benefit of preventing post-MI depression, an independent predictor of mortality. This study tested the efficacy and safety of bupropion SR for smoking cessation in adult smokers hospitalized with MI or unstable angina. To do so, we conducted a five-site randomized double-blind placebo-controlled trial to determine whether bupropion SR, initiated in the hospital and continued for 12 weeks, was effective and safe when added to comprehensive cognitive-behavioral smoking counseling. The primary outcome measure was biochemically-confirmed 7-day point prevalence tobacco abstinence at 1 year follow-up. Principal secondary outcome measure was biochemically-confirmed 7-day point-prevalence at end-of-treatment (12 weeks). Secondary aims were to test whether bupropion SR delays the time to smoking relapse, reduces CHD morbidity and depressive symptoms, and improves health-related quality of life over 1 year of follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking, Myocardial Infarction, Unstable Angina, Cardiovascular Disease
Keywords
Smoking cessation, Bupropion SR, Hospital intervention, Myocardial infarction, Unstable angina

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
248 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
bupropion SR (sustained-release)
Primary Outcome Measure Information:
Title
Cotinine-validated 7-day point prevalence tobacco abstinence at 1 year follow-up
Title
Cotinine-validated 7-day point prevalence tobacco abstinence at 3 month follow-up (end of treatment)
Secondary Outcome Measure Information:
Title
Combined fatal and nonfatal cardiovascular events at 3 month follow-up (end of treatment)
Title
Combined fatal and nonfatal cardiovascular events at 1 year follow-up
Title
Cardiovascular mortality at 1 year follow-up
Title
Blood pressure elevation (SBP>160 or DBP>100) during treatment with study drug

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >18 years old, had smoked >1 cigarette in the past month, were admitted to the hospital with a diagnosis of acute cardiovascular disease (see below) had an expected hospital stay of >24 hours. Eligible admission diagnoses included (1) acute ischemic coronary heart disease (MI or unstable angina), (2) coronary artery bypass graft surgery, or (3) other cardiovascular conditions (congestive heart failure, cardiac arrhythmia, valvular heart disease, or atherosclerotic disease of the aorta, carotid, renal or peripheral arteries) in subjects with documented coronary artery disease. Exclusion Criteria: not willing to consider smoking cessation after discharge, a contraindication to bupropion (seizure disorder, monoamine oxidase inhibitor use, history of anorexia nervosa or bulimia, bupropion allergy) a condition that increased the risk of seizure (e.g., serious head trauma with loss of consciousness uncontrolled hypertension (BP >160/100) in hospital heavy alcohol use (>3 drinks/day) or binge drinking (>6 drinks for males or >5 drinks for females) at least monthly renal insufficiency (serum creatinine >2.0 mg/dl), severe hepatic disease severe depression or severe cognitive impairment or psychosis life expectancy of <12 months, illegal drug use in the past 6 months bupropion use in the past month non-English speaking no telephone residence outside a defined geographic area.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy A Rigotti, MD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18227366
Citation
Thorndike AN, Regan S, McKool K, Pasternak RC, Swartz S, Torres-Finnerty N, Rigotti NA. Depressive symptoms and smoking cessation after hospitalization for cardiovascular disease. Arch Intern Med. 2008 Jan 28;168(2):186-91. doi: 10.1001/archinternmed.2007.60.
Results Reference
derived
PubMed Identifier
17145253
Citation
Rigotti NA, Thorndike AN, Regan S, McKool K, Pasternak RC, Chang Y, Swartz S, Torres-Finnerty N, Emmons KM, Singer DE. Bupropion for smokers hospitalized with acute cardiovascular disease. Am J Med. 2006 Dec;119(12):1080-7. doi: 10.1016/j.amjmed.2006.04.024.
Results Reference
derived

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Bupropion for Hospitalized Smokers With Acute Cardiovascular Disease

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