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Clinical Trials in the EU / 2025-524194-17-00
Authorised Phase III

EFFICACY OF PROPRANOLOL IN TRAUMATIC BRAIN INJURY PATIENTS ADMITTED TO THE ICU: A PROSPECTIVE, RANDOMIZED, TRIPLE-BLIND STUDY (ProP TBI in ICU)

2025-524194-17-00 · tracked via the Priya Life Science EU tracker
Sponsor
University Hospital Son Espases
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Nervous System Diseases
Decision date
05/02/2026
Enrollment target
600
Sites
Spain

Condition studied

Head injury

Investigational medicinal product(s)

METHYLCELLULOSEPropranolol 10 mg Tablets

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

Hospital mortality

Endpoint detail

Glasgow outcome scale extended

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-524194-17-00 on CTIS ↗ ← All trials in the EU