Beta-Adrenergic Modulation of Drug Cue Reactivity

NCT05587361 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-04-28

No results posted yet for this study

Summary

This study is designed to investigate the effects of a beta-adrenergic antagonist (Propranolol; 40 mg IR) and nicotine patch (14 mg) administered alone and in combination on neurobiological and behavioral responses to smoking cues in ongoing cigarette smokers. This is a basic experimental study in humans and participants will not take these medications for an extended period or make a cessation attempt as part of their involvement in this research project.

Conditions

  • Tobacco Use Disorder
  • Nicotine Dependence
  • Cigarette Smoking

Interventions

DRUG

Propranolol

Propranolol Capsule; 40 mg IR

DRUG

Nicotine Patch

Nicotine Patch; 14 mg

DRUG

Placebo Propranolol

Placebo Capsule, no active ingredients

DRUG

Placebo Patch

Placebo Patch, no active ingredients

Sponsors & Collaborators

  • Oklahoma State University Center for Health Sciences

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • National Institutes of Health (NIH)

    collaborator NIH
  • University of Oklahoma

    lead OTHER

Principal Investigators

  • Jason A Oliver, PhD · University of Oklahoma

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-26
Primary Completion
2027-03-31
Completion
2027-03-31
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05587361 on ClinicalTrials.gov