Effect of Progesterone on Smoking Behavior in Male and Female Smokers

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Mehmet Sofuoglu, Yale University
ClinicalTrials.gov Identifier:
NCT00271206
First received: December 28, 2005
Last updated: July 24, 2012
Last verified: July 2012

December 28, 2005
July 24, 2012
September 2004
September 2008   (final data collection date for primary outcome measure)
  • Smoking topography; measured by carbon monoxide levels and self-report at Day 4 [ Time Frame: 4 years anticipated ] [ Designated as safety issue: No ]
  • Nicotine withdrawal symptoms; measured by the Minnesota Nicotine Withdrawal Scale at Day 4 [ Time Frame: Anticipated 4 year study ] [ Designated as safety issue: No ]
  • Smoking topography; measured by carbon monoxide levels and self-report at Day 4
  • Nicotine withdrawal symptoms; measured by the Minnesota Nicotine Withdrawl Scale at Day 4
Complete list of historical versions of study NCT00271206 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Effect of Progesterone on Smoking Behavior in Male and Female Smokers
Progesterone and the Effects of Nicotine

Past research on nicotine addiction has shown that changes in estradiol and progesterone hormone levels during menstruation may cause women to respond differently than men to nicotine. The purpose of this study is to examine the effects of progesterone on smoking behavior, nicotine withdrawal symptoms, and the reinforcing effects of smoking in men and women addicted to nicotine.

Nicotine addiction is a serious health problem. Almost 35 million people in the United States try to quit smoking each year, but less than 7 percent are successful. Many smokers report a "high" sensation, followed by a feeling of relaxation. Such positive reinforcement factors, combined with nicotine cravings, make it difficult to stop the use of nicotine products. Past research has suggested that women may experience fewer nicotine cravings and may be less affected by smoking's positive reinforcement factors when compared to men. Fluctuations in levels of the female hormones estradiol and progesterone during menstruation may play a role in determining how women are affected by nicotine. The purpose of this study is to examine the effects of a controlled oral dose of progesterone on smoking behavior, nicotine withdrawal symptoms, and nicotine-related positive reinforcement factors in nicotine dependent males and females.

In this 4-day study, participants will be randomly assigned to receive a daily dose of 200 mg of progesterone, 400 mg of progesterone, or placebo. All participants will abstain from smoking for Days 1 through 3. On Day 4, participants will take part in a smoking session, during which their smoking habits, including the number of puffs, duration of puffs, and number of cigarettes smoked, will be measured. Outcome measurements will include self-reports of cravings; carbon monoxide monitoring; and standardized questionnaires to assess nicotine withdrawal symptoms.

This study has been completed with 35 men and 30 women. With the final women completing in March of 2008. This protocol is complete and has been published.

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Tobacco Use Disorder
  • Drug: Progesterone
    compared to placebo
  • Drug: sugar pill
    Compared to progesterone
  • Active Comparator: Progesterone
    200 mg to 400mg of progesterone
    Intervention: Drug: Progesterone
  • Placebo Comparator: Sugar Pill
    Will mirror active medication
    Intervention: Drug: sugar pill
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
65
September 2008
September 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • History of smoking 10-25 cigarettes daily for the past 12 months
  • Score of at least 5 on the Fagerström Nicotine Tolerance Questionnaire
  • Carbon monoxide level greater than 10 ppm
  • Body mass index between 19 to 36
  • Currently in good health, as determined by medical history, screening examination, and laboratory tests
  • If female, regular menstrual cycle every 25 to 35 days
  • If female, willing to use non-hormonal contraception throughout the study

Exclusion Criteria:

  • Seeking treatment for nicotine dependence
  • History of major medical illness, including liver disease; abnormal vaginal bleeding; suspected or known tumors; thrombophlebitis; deep vein thrombosis; pulmonary embolus; clotting or bleeding disorders; heart disease; diabetes; stroke; or other medical conditions that are considered unsafe for study participants by the investigator
  • Regular use of psychotropic medication (antidepressants, antipsychotics, or anxiolytics)
  • Recent diagnosis and treatment for Axis I disorders, including major depression, bipolar affective disorder, schizophrenia, or panic disorder
  • Currently abusing alcohol or other recreational or prescription drugs
  • Current use of any tobacco products other than cigarettes, including smokeless tobacco and nicotine products
  • Known allergy to progesterone
  • Known allergy to peanuts
  • If female, amenorrhea
  • Pregnant or breastfeeding
Both
18 Years to 40 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00271206
R01 DA014537, R01DA014537, DPMC
Yes
Mehmet Sofuoglu, Yale University
Yale University
National Institute on Drug Abuse (NIDA)
Principal Investigator: Mehmet Sofuoglu, PhD Yale University, Department of Psychiatry
Yale University
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP