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RecruitingAccepts healthy volunteersPhase 4

Beta-Adrenergic Modulation of Drug Cue Reactivity

University of Oklahoma · with Oklahoma State University Center for Health Sciences, Duke University · NCT05587361

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 21–60 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 4
Target enrollment
80
US sites recruiting
1
Study start
November 26, 2024
Record last updated
April 28, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Propranolol; Nicotine Patch; Placebo Propranolol; Placebo Patch

Conditions: Tobacco Use Disorder; Nicotine Dependence; Cigarette Smoking

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Generally healthy
  • Age 21-60
  • Right-handed using a three-item scale
  • Daily smoker of ≥ 5 cigarettes/day delivering 0.5 mg nicotine (FTC)
  • Smoking regularly for ≥ 1 year, with stable smoking for the past 6 months
  • Afternoon expired Carbon Monoxide (CO) concentration ≥ 6 ppm and/or morning urinary cotinine >100 ng/ml
  • Must identity at least 4 different smoking locations used in a typical week
  • Able to read and understand English

Exclusion Criteria

  • Inability to attend all required sessions
  • Significant health problems that would preclude active participation
  • Presence of conditions that would make MRI unsafe (e.g. pacemaker) or (e.g. weight and body shape)
  • Current use of psychoactive medications/drugs as indicated by self-report or urine screen
  • Positive breath alcohol concentration
  • Pregnant, breastfeeding, or planning to become pregnant during the course of the study (females)
  • Problems with vision that cannot be corrected with contacts or glasses
  • Current regular use of smokeless tobacco, smoking cessation medications, or other nicotine containing products (e.g. electronic cigarettes)
  • Current use of beta-adrenergic medications (e.g. beta-blockers) or other blood pressure medications
  • Systolic blood pressure \< 90 mmHg or diastolic blood pressure \< 60 mmHg (sitting or standing)
  • Abnormal EKG
  • Presence of severe anemia
  • Presence of electrolyte imbalance that could impact blood pressure
  • Presence of any other contraindications for propranolol or nicotine patch (e.g. cardiovascular disease, bronchial asthma, prior allergic reactions, diabetes)

Recruiting US locations

  • Hardesty Center for Clinical Research and Neuroscience

    Tulsa, OK 74136

    Site contact: Isabel Brush, B.A. · Isabel-Brush@ouhsc.edu

Study contacts (from the official record)

  • Jason A Oliver, PhD · 405-271-8001 · Jason-Oliver@ouhsc.edu
  • Isabel Brush, B.A. · Isabel-Brush@ouhsc.edu
Beta-Adrenergic Modulation of Drug Cue Reactivity (NCT05587361) | Bored Studies