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Adrenergic blockade in adult burns patients

The effect of adrenergic blockade on hypermetabolism in patients post burn injury

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000550909
Enrollment
26
Registered
2011-05-31
Start date
2011-06-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Post burn injury, survivors undergo a “hypermetabolic” response resulting in loss of muscle mass and increase in fat tissue, increased cardiac work, and delays in wound healing. Consequently these patients have weakness, increased length of hospital stay decreased functional ability and delayed return to work rates. One way to counteract this problem is by pharmacological blockade ie using medication to block the hypermetabolic response. One drug that has been trialled extensively in paediatrics are beta - blockers which decrease the work of the heart. The studies in children have shown these drugs can improve donor site and graft healing, attenuate muscle mass loss, prevent loss of lean muscle mass, improve immune function and decrease in the high temperature, high heart rate, increased cardiac work, and fatty infiltration of the liver. There have been two small trials in adults who did not blind investigators, investigate long term factors and included patients with burns less than 30% total body surface area. We plan to complete a single blinded, randomized trial on beta -adrenergic blockade in large severe adult burns patients investigating a number of important long term outcomes including lean muscle mass, cardiac function, wound healing, exercise capacity and metabolic profile. The specific aim is to investigate whether Propranolol)1mg/kg/day) a nonselective beta(1,) beta(2)-receptor antagonist, can prevent the loss of lean muscle mass and improve cardiac function, wound healing, exercise capacity and metabolic profile following severe thermal injury

Interventions

The medication propranolol hydrochloride for 30 days with 1mg/kg/day in four divided doses titrated upwards to decrease resting heart rate by 20%

Sponsors

Burns, Trauma & Critical Care Research Centre
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Acute burns patients 18years of age and over 30% total burns surface area, Ready for discharge from intensive care, at a stage when they do not require inotropic support, are non septic, antibiotic free and capable of spontaneous breathing on a high flow humidifier

Exclusion criteria

Concomitant multi-trauma, Pregnancy, Lactation, A premorbid history of asthma or bronchospasm, Peripheral arterial disease, Diabetes, Systolic blood pressure<100mmHg or mean arterial pressure of < 65mmHg, Heart rate<60bpm, Heart block on ECG, Previous use of beta blockers before the burn injury, or previous prescription for greater than 24 hours within the preceding 24 hours, Allergic disorders Any cardiovascular conditions (hypertension, coronary artery disease, left ventricular systolic impairment, pulmonary hypertension, right ventricular impairment, sick sinus syndrome, heart block), Renal or hepatic impairment, Hyperthyroidism, Previous depressive illness Compassionate care only

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026