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Fluoxetine as a Quit Smoking Aid for Depression-Prone Smokers

Primary Purpose

Depression, Smoking

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Fluoxetine
Behavioral group smoking cessation treatment
Placebo
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Depression, Fluoxetine, Nicotine dependence

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Subjects will be 144 smokers who have experienced at least one episode of major depressive disorder and 206 smokers who lack a lifetime history of major depressive disorder. None will currently meet diagnostic criteria for major depression, nor will they have met criteria in the past 6 months. All will be male and female community members between the ages of 18 and 65 who have smoker at least 10 cigarettes a day for the past year. Exclusion Criteria: Subjects may not enter the trial if they: have taken monoamine oxidase inhibitors, antidepressants, anti-anxiety agents, lithium, tryptophan or phenothiazines within the past month; are being treated for hypertension with guanethidine, reserpine, thiazide diuretics, beta blockers, or clonidine; are taking Type IC antiarrhythmics (e.g., propafenone and flecanide) or a highly protein-bound drug (e.g., warfarin, digitoxin); have a medically unstable condition or had a major health event in the past 6 months (e.g., myocardial infarct or major surgery); have CBC values more than 10% outside the normal limits, or liver enzymes exceeding 40% of the upper limit of normal; have a history of severe allergies, multiple adverse drug reactions or known allergy to fluoxetine; are actively abusing alcohol or drugs or received inpatient treatment for substance abuse within the past year; are using nicotine replacements; are pregnant, lactating, or of childbearing potential; present current evidence of organic brain disease, definite or subclinical major depressive disorder or serious suicidal risk post-traumatic stress disorder, or premenstrual dysphoric disorder; have a score greater than 14 on the 21-item Hamilton Depression Rating Scale or greater than 15 on the Beck Depression Inventory; have a history of seizures, mania or hypomania, or psychosis. Individuals with bipolar disorder, PTSD, or schizophrenia will be excluded because they might respond adversely to fluoxetine. Subjects with dysthymic disorder or anxiety disorders will be studied if their current symptoms are not sequelae of an episode of major depression. Excluding such cases would purify the sample by removing mild degrees of dysphoria, but would greatly restrict our ability to generalize any treatment implications to the current population that smokers.

Sites / Locations

  • Edward Hines, Jr. VA Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

tobacco abstinence

Secondary Outcome Measures

Full Information

First Posted
July 3, 2001
Last Updated
February 26, 2009
Sponsor
US Department of Veterans Affairs
Collaborators
Eli Lilly and Company
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1. Study Identification

Unique Protocol Identification Number
NCT00018174
Brief Title
Fluoxetine as a Quit Smoking Aid for Depression-Prone Smokers
Official Title
Fluoxetine as a Quit Smoking Aid for Depression-Prone Smokers
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
February 1998 (undefined)
Primary Completion Date
January 2003 (Actual)
Study Completion Date
January 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
US Department of Veterans Affairs
Collaborators
Eli Lilly and Company

4. Oversight

5. Study Description

Brief Summary
This project is a treatment-matching study to test whether adding antidepressant pharmacotherapy to behavioral cessation treatment improves the depression-prone smoker's ability to quit, while not undermining cessation goals for the smoker who lacks a history of depression. The study target is to randomize 120 smokers with a prior history of depression and 120 smokers who lack such a history to a double-blind treatment with either 60 mg fluoxetine or placebo, while they undergo cognitive behavioral treatment to quit smoking.
Detailed Description
The aim of this research is to examine whether adding antidepressant pharmacotherapy to behavioral cessation treatment improves the depression-prone smoker's ability to quit, while not undermining cessation for the smoker who lacks a history of depression, by randomizing smokers both with and without such a history to double-blind treatment with either 60 mg fluoxetine or placebo. The primary Depressive Episode Hypothesis states that the stress of quitting smoking and the biological challenge of nicotine withdrawal trigger a depressive episode in vulnerable individuals. To the extent that episode onset can be prevented by prophylactic administration of antidepressant pharmacotherapy, smokers with a history of depression will show significantly higher abstinence rates when treated with fluoxetine than placebo, whereas no drug effect will be evident for history negative smokers who lack the depressive diathesis. An alternative generalized withdrawal hypothesis construes post-cessation dysphoria as one general manifestation of a nicotine withdrawal syndrome that occurs independently of depressive vulnerability, and predicts that fluoxetine, as compared to placebo, will uniformly improve cessation outcomes, regardless of whether smokers possess the diathesis for depression. Over period of four years, the study hopes to randomize 120 smokers with a history of depression and 120 smokers who lack such a history to double-blind treatment with either 60 mg fluoxetine or placebo, while they undergo group cognitive behavioral treatment to quit smoking. To allow plasma drug levels to stabilize before quitting smoking, drug or placebo treatment begins 3 weeks before quitting smoking and continues for an additional 8 weeks following the quit date. Participants will be followed up monthly for 4 months after the end of treatment in order to assess the main study outcome; abstinence from smoking 6 months after the quit date.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Smoking
Keywords
Depression, Fluoxetine, Nicotine dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
247 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Intervention Type
Behavioral
Intervention Name(s)
Behavioral group smoking cessation treatment
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
tobacco abstinence
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects will be 144 smokers who have experienced at least one episode of major depressive disorder and 206 smokers who lack a lifetime history of major depressive disorder. None will currently meet diagnostic criteria for major depression, nor will they have met criteria in the past 6 months. All will be male and female community members between the ages of 18 and 65 who have smoker at least 10 cigarettes a day for the past year. Exclusion Criteria: Subjects may not enter the trial if they: have taken monoamine oxidase inhibitors, antidepressants, anti-anxiety agents, lithium, tryptophan or phenothiazines within the past month; are being treated for hypertension with guanethidine, reserpine, thiazide diuretics, beta blockers, or clonidine; are taking Type IC antiarrhythmics (e.g., propafenone and flecanide) or a highly protein-bound drug (e.g., warfarin, digitoxin); have a medically unstable condition or had a major health event in the past 6 months (e.g., myocardial infarct or major surgery); have CBC values more than 10% outside the normal limits, or liver enzymes exceeding 40% of the upper limit of normal; have a history of severe allergies, multiple adverse drug reactions or known allergy to fluoxetine; are actively abusing alcohol or drugs or received inpatient treatment for substance abuse within the past year; are using nicotine replacements; are pregnant, lactating, or of childbearing potential; present current evidence of organic brain disease, definite or subclinical major depressive disorder or serious suicidal risk post-traumatic stress disorder, or premenstrual dysphoric disorder; have a score greater than 14 on the 21-item Hamilton Depression Rating Scale or greater than 15 on the Beck Depression Inventory; have a history of seizures, mania or hypomania, or psychosis. Individuals with bipolar disorder, PTSD, or schizophrenia will be excluded because they might respond adversely to fluoxetine. Subjects with dysthymic disorder or anxiety disorders will be studied if their current symptoms are not sequelae of an episode of major depression. Excluding such cases would purify the sample by removing mild degrees of dysphoria, but would greatly restrict our ability to generalize any treatment implications to the current population that smokers.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bonnie Spring, PhD
Organizational Affiliation
Edward Hines Jr. VA Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Edward Hines, Jr. VA Hospital
City
Hines
State/Province
Illinois
ZIP/Postal Code
60141-3030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17295567
Citation
Spring B, Doran N, Pagoto S, McChargue D, Cook JW, Bailey K, Crayton J, Hedeker D. Fluoxetine, smoking, and history of major depression: A randomized controlled trial. J Consult Clin Psychol. 2007 Feb;75(1):85-94. doi: 10.1037/0022-006X.75.1.85.
Results Reference
result

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Fluoxetine as a Quit Smoking Aid for Depression-Prone Smokers

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