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Non-Nicotine Agents for Smoking Cessation

US Department of Veterans Affairs (VA) logo

US Department of Veterans Affairs (VA)

Status and phase

Completed
Phase 3

Conditions

Tobacco Use Disorder

Treatments

Drug: transdermal patch and nicotine inhaler
Drug: bupropion and transdermal patch

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT00108537
ADRD-013-01S

Details and patient eligibility

About

The primary objective of this study is to determine which is the better approach to smoking cessation in veterans: bupropion combined with transdermal nicotine or high dose nicotine replacement therapy (NRT) using transdermal nicotine combined with nicotine inhaler.

Full description

This study is a two-arm open-label, randomized controlled trial of bupropion combined with transdermal nicotine versus high dose NRT (transdermal nicotine and nicotine inhaler) with all subjects receiving a behavioral counseling program for smoking cessation.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Readiness to set a quit date in the next two weeks,
  • Current smoking of at least 15 cigarettes a day

Exclusion criteria

  • Current untreated depression or receiving treatment for depression,
  • History of seizures, major head injury, or other predisposition for seizures

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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