Status:
COMPLETED
Smoking Cessation and Sexual Health in Men
Lead Sponsor:
University of Texas at Austin
Conditions:
Smoking Cessation
Eligibility:
MALE
23-60 years
Phase:
PHASE1
Brief Summary
This is a 12-week clinical trial investigating the effects of smoking cessation on sexual functioning in men. This study consists of 3 sessions and provides 8 weeks of free nicotine transdermal patche...
Detailed Description
Objective: Tobacco use constitutes the single most preventable cause of disease and death in the world today and is responsible for introducing a number of diseases including many types of cancer, car...
Eligibility Criteria
Inclusion
- Male
- Between the ages of 25 and 60
- Proficient in English
- Currently smoke at least 15 cigarettes per day for at least 5 years
- Heterosexual
- Currently sexually active (sexual intercourse within the past 30 days)
- Committed to quit smoking
Exclusion
- History of HIV infection or active, untreated pelvic or urinary tract infection including, sexually transmitted diseases such as chlamydia genital herpes, gonorrhea, or syphilis.
- Major pelvic surgery that may have caused nerve damage, or serious bladder, rectal, or abdominal surgery.
- Neurological impairment due to diabetes, stroke, pelvic nerve damage secondary to trauma, cancer treatments, myasthenia gravis, multiple sclerosis or spinal cord damage.
- Clinically significant untreated renal or endocrine disease.
- Uncontrolled hypotension or hypertension manifested by systolic blood pressure \>170 or \<90 mm Hg or diastolic blood pressure \>100 or \<50 mm Hg.
- History of serious drug abuse or serious alcohol abuse within the past 12 months (\>= 16 points on the Alcohol Use Disorders Identification Test (AUDIT) and \>= 6 on the Drug Abuse Screening Test (DAST-10).
- Evidence of schizophrenia, bipolar disorder, delusional disorder, or psychotic disorders not classified elsewhere as per the DSM-IV
- Using medications known to affect sexual or vascular functioning, including antidepressants and anti-hypertensives, as well as sildenafil, vardenafil, tadalafil, or any other substance designed to affect sexual performance
- Patients using insulin, narcotic pain relievers (propoxyphene, pentazocine), tricyclic antidepressants, oxazepam, or medications for respiratory diseases such as COPD or asthma (xanthines (e.g., theophylline) as these drugs are contraindicated by the nicotine patch
- Patients who report experiencing clinically significant sexual difficulties, including hypoactive sexual desire disorder, sexual arousal disorder, premature ejaculation, or inhibited orgasm prior to the onset of smoking.
- Recent myocardial infarction, serious heart arrhythmias, and those with serious or worsening angina.
- Hypersensitivity or allergy to nicotine.
- History of or current psoriasis, dermatitis (atopic or eczematous), active peptic ulcers, severe renal impairment, hyperthyroidism, pheochromocytoma, or insulin-dependent diabetes mellitus.
Key Trial Info
Start Date :
December 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2010
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT00833404
Start Date
December 1 2008
End Date
December 1 2010
Last Update
September 12 2011
Active Locations (1)
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1
University of Texas at Austin
Austin, Texas, United States, 78712