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Burns clinical trials

View clinical trials related to Burns.

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NCT ID: NCT01501097 Active, not recruiting - Sepsis Clinical Trials

The Impact of Continuous Renal Replacement Therapy on the Outcomes of Burn Patients With Early Phase of Sepsis

CRRT
Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if early application of CRRT will result in an improvement of clinical outcomes of burn patients during the early phase of sepsis

NCT ID: NCT01368367 Active, not recruiting - Burns Clinical Trials

Exercise Training Post Burn Injury

Start date: December 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a high intensity aerobic and resisted exercise program will improve physical, functional and psychological outcomes in patients post burn injury.

NCT ID: NCT01299753 Active, not recruiting - Burns Clinical Trials

Catecholamine Blockade Post-burn

Start date: February 2011
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT01213914 Active, not recruiting - Burns Clinical Trials

Hemofiltration in Burns: RESCUE (Randomized Controlled Evaluation of Hemofiltration in Adult Burn Patients With Septic Shock and Acute Renal Failure)

RESCUE
Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is determine if High-Volume Hemofiltration in addition to 'contemporary' care will result in an improvement of select clinical outcomes when compared to 'contemporary' care alone in the treatment of critically ill patients with ARF secondary to septic shock.

NCT ID: NCT00985205 Active, not recruiting - Burns Clinical Trials

The RE-ENERGIZE Study: RandomizEd Trial of ENtERal Glutamine to minimIZE Thermal Injury

RE-ENERGIZE
Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the following hypotheses: 1. Enteral glutamine administration decreases in-hospital mortality in adult patients with severe thermal burn injuries. 2. Enteral glutamine administration decreases hospital-acquired blood stream infections from Gram negative organisms and length of stay in ICU and hospital for adult patients with severe thermal burn injuries. 3. Enteral glutamine administration will improve the physical function of surviving burn injured patients and reduce their cost of care. The objectives of this trial are to determine the overall treatment effect and safety of glutamine in burn patients. Specifically, the investigators want to assess the following outcomes in a sample of 1200 patients in 80 sites: 1. In patients with severe, life-threatening burn injury, what is the effect of enteral glutamine on time to discharge alive from hospital 2. In patients with severe, life-threatening burn injury, what is the effect of enteral glutamine on 6 month mortality, hospital-acquired blood stream infections from Gram negative organisms, hospital mortality, duration of stay in ICU and hospital, health-related quality of life, and health care resources?

NCT ID: NCT00689650 Active, not recruiting - Burn Scar Patients Clinical Trials

Fractional Nonablative 1540 nm Laser Resurfacing for Burn Scars- A Randomised Controlled Trial

Start date: November 2007
Phase: N/A
Study type: Interventional

The objective was to evaluate the efficacy of 1540 nm fractional laser treatment of mature burn scars.

NCT ID: NCT00558701 Active, not recruiting - Burns Clinical Trials

Microcurrent for Healing Autogenous Skin Donor Sites

Start date: December 2007
Phase: N/A
Study type: Interventional

A decrease in donor site wound healing time (as assessed by the research team) of 2 days will be observed with the addition of active microcurrent to silver- coated nylon dressing.

NCT ID: NCT00369876 Active, not recruiting - Burns Clinical Trials

Anorexia in Children With Burn Injury and the Reactions of the Immune and Endocrine Systems

Start date: August 2004
Phase: Phase 1
Study type: Observational

Anorexia in children with burn injury is a common phenomenon. The study is searching for the origin of the anorexia in those children. The study correlates between the level peptides of the immune and the endocrine systems and the length of the anorexia.