Clinical Trials Directory

Trials / Terminated

TerminatedNCT00356187

Beta Blockade in Critical Injury

Beta-blockade Reduces Catabolism in Severely Injured Trauma Patients

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Denver Health and Hospital Authority · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Critically injured patients endure a period of hypermetabolism/catabolism after being resuscitated. The metabolic cost of this may be measured in loss of lean body mass, poor wound healing, susceptibility to infection and long hospital stays. While there have been some data to suggest that hypermetabolism can be ameliorated in burn patients by beta blockade, to our knowledge, a prospective trial in trauma patients has not yet been done. Our hypothesis is that nonselective beta blockade will reduce catabolism, improve glucose control, blunt loss of lean body mass, decrease infections and improve outcome in a cohort of critically injured patients.

Conditions

Interventions

TypeNameDescription
DRUGPropranolol

Timeline

Start date
2006-02-15
Primary completion
2009-01-31
Completion
2009-01-31
First posted
2006-07-25
Last updated
2018-03-15
Results posted
2018-02-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT00356187. Inclusion in this directory is not an endorsement.