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Burn clinical trials

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NCT ID: NCT00324311 Completed - Burn Clinical Trials

Enzymatic Debridement in Burns Patients: A Comparison to Standard of Care

Start date: December 2005
Phase: Phase 3
Study type: Interventional

Burns represent one of the most severe and dreaded traumas. Burned and traumatized tissue is known as eschar. The dead eschar, if not removed, often becomes heavily contaminated and is the source of local and/or systemic infection or sepsis. The local inflammation and infection destroy healthy surrounding tissues and extends the original damage. In order to prevent these complications, and in order to minimize the risk of infection, it is imperative to evaluate the burn and remove all of the offending eschar at the earliest possible opportunity. This removal of dead tissue is termed "debridement". The most direct debridement method for eschar removal is surgery. Traditional, conservative non-surgical debridement is a lengthy process which often involves many complications. The objective of this study is to evaluate the safety and enzymatic debriding efficacy of Debrase Gel Dressing (DGD) in hospitalized patients with deep partial thickness and/or full thickness thermal burns and to compare DGD to standard of care (SOC).

NCT ID: NCT00294697 Recruiting - Sepsis Clinical Trials

Genetic Variation and Immune Responses After Injury

Start date: August 2003
Phase: N/A
Study type: Observational

Our overall hypothesis is that genetic variations in innate immunity genes predispose patients to varying responses after injury by altering the systemic and local inflammatory responses. In addition, we hypothesize that these genetic differences are associated with different clinical outcomes

NCT ID: NCT00285636 Completed - Burn Clinical Trials

Long Term Follow-Up of Burn Injuries

Start date: June 1992
Phase: N/A
Study type: Observational

The purpose of the study is to investigate the psychological effects of burn injuries as experienced by patients.

NCT ID: NCT00285090 Terminated - Malnutrition Clinical Trials

Bone Mineral Density, Body Composition and Growth Following Severe Burn Injury

Start date: February 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is two-fold. The first is to establish that bone mineral density is diminished among children admitted to this regional burn center as compared to healthy non-burned children. The second purpose of this study is to examine the short and long-term effects of calcium and vitamin D supplementation in on bone metabolism and accrual in children who have been burned. Specific Aims: 1) To measure bone mineral content and bone mineral density and their change during growth in convalescent burned children admitted to a regional burn center and to compare them to normal, healthy children.; 2) To measure lean body mass, fat mass, total body water in convalescent burned children admitted to a regional burn center and compare them to normal, healthy children with focus on how these components of body composition relate to indices of bone mineral content and density; 3) To identify alterations in bone metabolism and calcium and vitamin D homeostasis following burn injury and relate these to bone mineral density in burned children; 4) To test the effect of short term calcium and vitamin D supplementation on improving bone mineral density, bone mineral content, and indices of calcium and vitamin D metabolism in acutely burned children.

NCT ID: NCT00261690 Completed - Burn Clinical Trials

Virtual Reality Pain Control During Burn Wound Care

VRPT/H2O/RT
Start date: February 2002
Phase: Phase 2/Phase 3
Study type: Interventional

Using Virtual Reality as a form of Distraction during Burn Care.

NCT ID: NCT00260221 Completed - Burn Clinical Trials

VRH Pain Reduction During Burn Wound Care and Physical Therapy

VRH
Start date: January 2002
Phase: N/A
Study type: Interventional

Using Virtual Reality Hypnosis to relief pain and anxiety for burn patients.

NCT ID: NCT00253279 Not yet recruiting - Burn Clinical Trials

Alterations in Protein Synthesis Rates of Burn Patients Measured Over Time Using PET Scans

Start date: November 2009
Phase: Phase 1
Study type: Observational

Our specific aim is to gain an understanding of protein synthesis rates in burn patients at various times during their injury and recovery by using PET scans. This will be compared with healthy volunteer controls. We hope this will help optimize nutrition and care regimens for future burn patients.

NCT ID: NCT00242970 Completed - Burn Clinical Trials

Hypertrophic Scarring After Facial Burn

Start date: October 2005
Phase: Phase 2
Study type: Observational

Subjects with a burn to the face and/or neck will be enrolled into the study and a Three-Dimensional scanner used to see if it can objectively measure scar color and volume and measure the effect of scar on motion of the face and neck.

NCT ID: NCT00239668 Completed - Burn Clinical Trials

Multicenter Benchmarking of Functional and Psychosocial Outcomes of Pediatric Burn Survivors

Start date: March 2000
Phase:
Study type: Observational

The purpose of this study is to establish an expected recovery trajectory (recovery model) in terms of physical and psychological function of the pediatric burn patient.