Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06982183

The Effects of Propranolol, Hydrocortisone, and Morphine on Military-Relevant Performance Outcomes

The Effects of Propranolol, Hydrocortisone, and Morphine on Military-Relevant Performance Outcomes: A Randomized, Blinded, Placebo Controlled Study

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Walter Reed Army Institute of Research (WRAIR) · Federal
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This clinical trial aims to evaluate the nature and duration of effects of three FDA-approved medications (propranolol, hydrocortisone, and morphine) on military-relevant cognitive, emotional, and motor performance following an exposure to a stressful situation (i.e., exposure to a tarantula) in physically healthy adult volunteers (aged 18 - 40) with fear of spiders to help the future development of medications for treating Acute Stress Reactions. The main questions this study aims to answer are: Will placebo treatment (oral placebo) result in significant decrements in Psychomotor Vigilance Task (PVT) performance compared to propranolol treatment? Will placebo treatment \[intramuscular (IM) placebo\] result in significant decrements in PVT performance compared to hydrocortisone treatment? Will placebo treatment (IM placebo) result in significant decrements in PVT performance compared to morphine treatment? Participants will receive one of five study medications (oral propranolol, oral placebo, IM hydrocortisone, IM morphine, or IM morphine) after a brief exposure to a tarantula. Participants will complete cognitive and simple motor tasks and psychological assessments before and after the study medication administration.

Conditions

Interventions

TypeNameDescription
DRUGPropranololAn administration of a 40-mg propranolol capsule immediately after tarantula exposure
DRUGHydrocortisoneAn intramuscular administration of 62.5 mg/1 ml of hydrocortisone immediately after tarantula exposure
DRUGMorphineAn intramuscular administration of 5 mg/1 ml of morphine immediately after tarantula exposure
DRUGPlacebo (oral)An administration of a placebo capsule after tarantula exposure
DRUGPlacebo (IM)An intramuscular administration of 1 ml of saline immediately after tarantula exposure

Timeline

Start date
2025-05-27
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2025-05-21
Last updated
2025-07-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06982183. Inclusion in this directory is not an endorsement.