Catecholamine Blockade Post-burn

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT01299753
Collaborator
(none)
80
1
2
154.9
0.5

Study Details

Study Description

Brief Summary

Severe burn is associated with a wide array of stress, metabolic, and physiologic processes in an attempt to restore homeostasis. The catecholamine induced stress response following severe burns is particularly exaggerated and manifests detrimentally as inflammation, insulin resistance, hypermetabolism, and associated profound protein catabolism. The investigators hypothesize that catecholamine blockade will lead to restored IR signaling and result in improved post-burn morbidity. The investigators will further determine the molecular mechanisms mediating these effects.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Clinical and Molecular Effects of Catecholamine Blockade Post-burn
Study Start Date :
Feb 1, 2011
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Control

Drug: placebo
identically packed placebo

Experimental: Beta blockade

Drug: propranolol
20-40 mg q6-8h

Outcome Measures

Primary Outcome Measures

  1. Perform oral glucose tolerance test [Conduct at week 1 post admission]

    Standard fasting oral glucose tolerance test with an intake of 75 g of glucose. Subsequent measurements (in mg/dl) of glucose in blood, insulin and c-peptide will be conducted over 2 hours.

  2. Perform oral glucose tolerance test [Conduct at week 3 post admission]

    Standard fasting oral glucose tolerance test with an intake of 75 g of glucose. Subsequent measurements (in mg/dl) of glucose in blood, insulin and c-peptide will be conducted over 2 hours.

  3. Perform oral glucose tolerance test [Conduct at discharge (1-4 months post admission depending on severity of injury)]

    Standard fasting oral glucose tolerance test with an intake of 75 g of glucose. Subsequent measurements (in mg/dl) of glucose in blood, insulin and c-peptide will be conducted over 2 hours.

Secondary Outcome Measures

  1. Measure concentrations of serum cytokines [weekly until discharge (1-4 months post admission depending on severity)]

    Inflammatory response will be assessed by measuring the concentrations (pg/ml) of a panel of serum cytokines (IL-1, IFN, TNF etc.) using the Bio-Plex 17-Plex Suspension assay.

  2. Record the episodes of Pneumonia [daily until discharge (1-4 months post admission depending on severity)]

    Pneumonia is defined by the following criteria: new progressive and persistent infiltrate, consolidation, or cavitations, in light of the baseline evaluation for inhalational injury on chest X-ray, along with signs of sepsis, worsening gas exchange (decreased P/F ratio), increased O2, and change in the sputum, e.g. purulent or increased sputum production.

  3. Record the episodes of sepsis [daily until discharge (1-4 months post admission depending on severity of injury)]

    Patients are evaluated daily and the number of episodes of sepsis or bloodstream infection will be recorded

  4. Measure the levels of activated signaling proteins using protein blotting [assess at 1st operation (week 1-2 post admission on average) and 3rd operation (week 3-4 post admission on average)]

    The level of activation of a protein signaling cascade (fold change compared to control), as indicated by the amount of phosphorylated protein substrates (e.g. p-Akt/Akt), will be measured in tissue obtained at operation using protein blotting techniques in the laboratory.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients between 18 and 90 years of age

  • 25% TBSA burn

Exclusion Criteria:
  • Death upon admission

  • Decision not to treat due to burn injury severity

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ross Tilley Burn Centre - Sunnybrook HSC Toronto Ontario Canada M4N 3M5

Sponsors and Collaborators

  • Sunnybrook Health Sciences Centre

Investigators

  • Principal Investigator: Marc G Jeschke, MD PhD, Sunnybrook Health Sciences Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Marc Jeschke, Principal Investigator, Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT01299753
Other Study ID Numbers:
  • Propran_Jeschke
First Posted:
Feb 18, 2011
Last Update Posted:
Mar 28, 2022
Last Verified:
Mar 1, 2022
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 28, 2022