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临床试验/NCT00129246
NCT00129246已完成1 期

Naltrexone & Bupropion to Stop Smoking With Less Weight Gain

Yale University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2004年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
1
主要终点
Weight Gain

研究概览

简要总结

This study will test a combination of the drugs naltrexone and bupropion with weight-concerned smokers to investigate whether or not this combination of drugs improves smoking cessation quit rates and minimizes post quit weight gain.

详细描述

This is an open label smoking cessation clinical trial of 25 mg naltrexone with 300 mg bupropion sustained-release (SR) in six male and fourteen female participants. This pilot study is being conducted to determine:

  • effect size estimates for smoking cessation and post-cessation weight gain, which will be used to compute the sample size needed for a large-scale clinical trial; and
  • compliance with a combination of 25 mg naltrexone and 300 mg bupropion SR. In addition to examining the sample in this study, the investigators plan to compare this sample to a sample of matched controls.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ages 18 and older
  • Willingness and ability to give written consent
  • Smoking at least 10 cigarettes per day for at least 1 year
  • Baseline expired carbon-monoxide level of at least 10 ppm
  • Weigh at least 100 lbs.
  • English-speaking
  • One person per household
  • At least 1 prior quit attempt
  • Concern about gaining weight. This will be assessed using a questionnaire that will provide a rating system to determine qualified participants.

排除标准

  • Pregnant or nursing women or women attempting to conceive
  • Serious current neurologic, psychiatric or medical illness, including unstable cardiac, hepatic, or renal disease and diabetes and hypertension
  • Current alcohol dependence
  • Current use of opiates, and/or a urine toxicology screen positive for opiates
  • Chronic pain conditions necessitating opioid treatment (naltrexone, an opioid antagonist will make these medications ineffective)
  • Evidence of significant hepatocellular injury as evidenced by AST or ALT >3 x normal or elevated bilirubin
  • History of cirrhosis
  • Body mass index (BMI) greater than 35
  • History of anorexia nervosa or bulimia
  • Current major depression
  • Currently taking Toprol-XL (or metoprolol succinate)
  • History of seizure disorder or serious brain injury
  • Current use of smokeless tobacco, pipes, cigars, nicotine gum, nicotine patch, nicotine inhaler, nicotine lozenge, nicotine nasal spray, or bupropion
  • Previous hypersensitivity to bupropion
  • Patients requiring concomitant therapy with any psychotropic drug
  • Participation in the Framing Messages for Smoking Cessation With Bupropion study (HIC#: 10880)

研究组 & 干预措施

Bupropion only

Active Comparator

The placebo comparator was a group of matched controls who received an identical psychosocial intervention and bupropion SR treatment regimen in a similar 7-week study investigation compared to naltrexone hydrochloride (25 mg/day) in combination with bupropion hydrochloride SR (300 mg/day).

干预措施: Bupropion (Drug)

Naltrexone +Bupropion

Experimental

The active comparator in this 7-week open label study investigation was naltrexone hydrochloride (25 mg/day) in combination with bupropion hydrochloride SR (300 mg/day) compared to matched controls who received an identical psychosocial intervention and bupropion SR treatment regimen (bupropion only).

干预措施: Naltrexone (Drug)

Naltrexone +Bupropion

Experimental

The active comparator in this 7-week open label study investigation was naltrexone hydrochloride (25 mg/day) in combination with bupropion hydrochloride SR (300 mg/day) compared to matched controls who received an identical psychosocial intervention and bupropion SR treatment regimen (bupropion only).

干预措施: Bupropion (Drug)

结局指标

主要结局

Weight Gain

时间窗: Week 6

Weight gain for for the entire sample in pounds at 6 weeks.

Point Prevalence Abstinence

时间窗: Week 6

Point prevalence abstinence is defined as the number of patients reporting point prevalence abstinence over the last 7 days.

Smoking Cessation

时间窗: Week 6

Smoking cessation is defined as the number of patients that displayed continuous 6-week abstinence from the quit date.

次要结局

  • Weight Gain Abstinent Participants(Week 6)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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