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Sibutramine to Reduce Weight Gain and Improve Smoking Cessation Rates (SUCCESS)
This study has been completed.
First Received: May 20, 2002   Last Updated: February 11, 2009   History of Changes
Sponsor: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier: NCT00037752
  Purpose

The purpose of this study is to determine if sibutramine will decrease post-cessation weight gain and cigarette smoking in overweight and obese smokers who quit smoking.


Condition Intervention
Cardiovascular Diseases
Heart Diseases
Obesity
Drug: Sibutramine
Behavioral: Behavioral Smoking Cessation Program

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Use of Sibutramine in Smoking Cessation

Resource links provided by NLM:


Further study details as provided by National Heart, Lung, and Blood Institute (NHLBI):

Primary Outcome Measures:
  • Post-cessation weight change [ Time Frame: Measured at 1 year follow-up ] [ Designated as safety issue: No ]
  • Smoking cessation [ Time Frame: Measured at 1 year follow-up ] [ Designated as safety issue: No ]

Enrollment: 436
Study Start Date: September 2002
Study Completion Date: August 2008
Primary Completion Date: August 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Active Comparator
Sibutramine plus a behavioral smoking cessation program
Drug: Sibutramine
At the baseline study visit, participants in Group 1 will be given a one month supply of 5 mg/d of sibutramine and a 1-month follow-up visit will be scheduled. After a safety evaluation at the 1-month follow-up visit, participants will have their dose of sibutramine titrated to 10 mg/d, a 1 month supply of the medication will be given to participants, and a 2-month follow-up visit will be scheduled. After a safety evaluation at the 2-month follow-up visit, participants will receive a 1 month supply of sibutramine 10 mg/d and a 3-month follow-up visit will be scheduled. At the 3-month follow-up visit, the sibutramine will be discontinued and participants will be scheduled for 4- and 5-month follow-up visits.
Behavioral: Behavioral Smoking Cessation Program
Both groups of participants will take part in a behavioral smoking cessation program.
2: Active Comparator
Placebo sibutramine plus a behavioral smoking cessation program
Behavioral: Behavioral Smoking Cessation Program
Both groups of participants will take part in a behavioral smoking cessation program.

Detailed Description:

BACKGROUND:

Cigarette smoking poses a serious but preventable health risk. Behavioral smoking cessation programs have been shown to help individuals quit smoking. However, concerns about post-cessation weight gain have been reported as a significant barrier to quitting for many smokers. Recently, sibutramine, a new serotonin and norepinephrine reuptake inhibitor drug, has received FDA approval to help people lose weight. Since sibutramine affects neurotransmitters that are important in regulating body weight, it is reasonable to hypothesize that it may decrease post-cessation weight gain in overweight and obese smokers who quit smoking. To date, there have been no studies that compare sibutramine to a placebo, as a way to reduce post-cessation weight gain among overweight and obese smokers who take part in a behavioral smoking cessation program. Therefore, whether sibutramine is effective at reducing post-cessation weight gain in these smokers is unknown. Further, given the neuropharmacologic effects of sibutramine, it is reasonable to speculate that this medication could also be effective in helping individuals quit smoking both initially and in the long term. It is possible that the use of sibutramine, as compared to placebo, may result in a decrease in post-cessation weight gain in overweight and obese individuals who quit smoking. The use of sibutramine may also result in an increase in smoking cessation rates.

DESIGN NARRATIVE:

This study tests the hypothesis that the use of sibutramine, as compared to placebo, will result in a decrease in post-cessation weight gain in overweight and obese individuals who quit smoking, and result in an increase in smoking cessation rates. Participants will be randomly assigned to one of the following two groups: 1) sibutramine plus a behavioral smoking cessation program; or 2) placebo sibutramine plus a behavioral smoking cessation program. Assessments will include post-cessation weight change and smoking cessation rates measured during the study and 9 months following the end of the study.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • In good general health
  • Body mass index greater than or equal to 25
  • Currently smoke cigarettes
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00037752

Locations
United States, Tennessee
University of Tennessee Health Science Center
Memphis, Tennessee, United States, 38163
Sponsors and Collaborators
Investigators
Principal Investigator: Karen C. Johnson, MD, MPH University of Tennessee Health Science Center
  More Information

No publications provided

Responsible Party: National Heart Lung and Blood Institute (NHLBI) ( Jared B. Jobe, PhD )
Study ID Numbers: 1176, R01 HL68049
Study First Received: May 20, 2002
Last Updated: February 11, 2009
ClinicalTrials.gov Identifier: NCT00037752     History of Changes
Health Authority: United States: Federal Government

Additional relevant MeSH terms:
Obesity
Heart Diseases
Psychotropic Drugs
Overweight
Pharmacologic Actions
Body Weight
Sibutramine
Signs and Symptoms
Anti-Obesity Agents
Therapeutic Uses
Nutrition Disorders
Appetite Depressants
Cardiovascular Diseases
Overnutrition
Central Nervous System Agents
Antidepressive Agents

ClinicalTrials.gov processed this record on November 27, 2009