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
| Type | Name | Description |
|---|---|---|
| DRUG | Propranolol |
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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT00356187. Inclusion in this directory is not an endorsement.