ClinicalTrials.gov record
Recruiting Phase 4 Interventional

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

ClinicalTrials.gov ID: NCT06982183

Public ClinicalTrials.gov record NCT06982183. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 9:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Study identification

NCT ID
NCT06982183
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 4
Lead sponsor
Walter Reed Army Institute of Research (WRAIR)
Federal
Enrollment
88 participants

Conditions and interventions

Interventions

  • Hydrocortisone Drug
  • Placebo (IM) Drug
  • Placebo (oral) Drug
  • Propranolol Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 40 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 26, 2025
Primary completion
Aug 31, 2026
Completion
Aug 31, 2026
Last update posted
May 12, 2026

2025 – 2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Sleep Research Center (SRC), Walter Reed Army Institute of Research Silver Spring Maryland 20910 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06982183, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 12, 2026 · Synced May 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06982183 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →