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The evaluation of the efficacy and safety of a transdermal delivery system of nicotine/mecamylamine in cigarette smokers

Completed
Conditions
Cigarette smoking
Not Applicable
Smoking
Registration Number
ISRCTN43027384
Lead Sponsor
Elan Corp (USA)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
375
Inclusion Criteria

1. Males or females motivated to quit smoking between the ages of 18 and 70 years
2. Smoked at least 20 cigarettes a day for three years or more (smoking confirmed via expired CO level >10 ppm).
All subjects had normal blood pressure and heart rate, weighed more than 100 pounds and typically no more than 130% of their ideal body weight, and expressed willingness to quit smoking on the specified target quit date (TQD). They were not currently using smokeless tobacco or other nicotine products. A detailed medical history, routine physical examination, laboratory tests and electrocardiogram (ECG) confirmed that subjects were in general good health. All women had a negative pregnancy test and agreed to use a medically accurate contraceptive method.

Exclusion Criteria

Participants were excluded if they had a history of significant hepatic, renal, endocrine, cardiac, psychiatric, gastrointestinal, pulmonary, or metabolic disorder including hyperthyroidism, pheochromocytoma, diabetes, severe coronary insufficiency, recent myocardial infarction (within 90 days), glaucoma, cerebrovascular disease, stroke, chronic renal failure, prostatic hypertrophy, prostatic disease, bladder neck obstruction, urine retention, urethral stricture, a history of atopic or eczematous dermatitis, psoriasis, or altered skin condition at patch application site.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Analysis of the four-week continuous abstinence for the intent-to-treat population using the slip definition, which allows smoking in the first two weeks after the quit date.
Secondary Outcome Measures
NameTimeMethod
Analysis of the four-week continuous abstinence for the intent-to-treat population using the strict definition (no smoking after the quit date).
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