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Burns clinical trials

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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.

NCT ID: NCT00220519 Terminated - Burns Clinical Trials

Lactobacillus GG Supplementation During Pediatric Burn Injuries

Start date: October 2004
Phase: N/A
Study type: Interventional

Critical illness and the therapies that accompany it are associated with a disruption in the ecological equilibrium of the GI tract that can ultimately lead to infection. Lactobacillus GG, a probiotic, replenishes the healthy flora of the intestinal tract and may decrease the risk of diarrhea and infection during critical illness. However, little is known about the impact of probiotics following a burn injury and the mechanisms behind the proposed benefits. The hypothesis of this research is that Lactobacillus GG decreases the incidence of diarrhea and infection in burned children receiving antibiotic therapy. The specific aim of this research is to determine the impact of Lactobacillus GG on the incidence of diarrhea and infection among burned children (>20% TBSA) receiving antibiotic therapy.

NCT ID: NCT00217035 Withdrawn - Burns Clinical Trials

Glutamine Enriched Total Parenteral Feeding and Proline Metabolism in Severely Burned Patients

Start date: August 1997
Phase: N/A
Study type: Observational

Proline is a non-essential amino acid that helps with collagen formation. Collagen is one of the main ingredients of skin, bone, tendons, and connective tissue. It is thought that proline becomes depleted in burn patients because it is being used in greater than normal quantities to help the injured skin and connective tissue heal. If this is true, then the body must look for alternate energy sources as proline becomes depleted. This study aims to evaluate 1)the metabolic kinetics of the amino acids proline, glutamate, and ornithine and 2) the effects of glutamine supplemented total parenteral nutrition (TPN) on the metabolism of these amino acids.

NCT ID: NCT00216996 Withdrawn - Burns Clinical Trials

Effect of Glutamine Supplemented Nutrition Support on Protein and Glutamine Metabolism in Burns

Start date: n/a
Phase: N/A
Study type: Observational

The Total Parenteral Nutrition (TPN)received as part of your routine burn care has optimal levels of protein and sugar, however the best mixture of amino acids for a patient with burn wounds is not yet known. Amino acids occur naturally in the body and the food we eat. The body combines amino acids to make protein. It uses the proteins to do things such as heal wounds, fight infection, and provide energy. We are studying if the body's use of protein is increased after receiving TPN containing the amino acid called glutamine. We hope to learn the best composition of TPN so that the body can more efficiently repair wounded tissues and recover earlier from an acute burn injury.

NCT ID: NCT00216983 Withdrawn - Burns Clinical Trials

Proline Metabolism in Severely Burned Patients: Effect of Modulated Parenteral Feeding

Start date: September 1997
Phase: N/A
Study type: Observational

The overall purpose of the study is to evaluate the effect of depleting proline supply in the nutritional support regimen on proline metabolism in the burn patients, this includes the rate of proline oxidation after burn injury, the rate of proline de novo synthesis from its immediate precursors glutamate and ornithine. The specific aims of the proposed study are: 1) to determine the kinetic status of proline metabolism and whole body proline balance under the following nutritional states: (a) "fasting; (b) regular total parenteral nutrition (TPN); (c)TPN with isonitrogenous depletion of proline, glutamate and ornithine metabolism under nutritional conditions studied in specific aim 1) above.

NCT ID: NCT00216970 Recruiting - Burns Clinical Trials

Study of Arginine Metabolism and Nitric Oxide Formation in Relation to Glutamine Supply in Severely Burned Patients

Start date: August 1997
Phase: N/A
Study type: Interventional

The purpose of the study is to understand the way the body uses amino acids and proteins in burned patient during the time they cannot eat normally. This study aims to understand the metabolism of the amino acid arginine in the body after burn injury. The results of this study will help determine the best composition of food needed during an acute burn injury so that body can more efficiently use the supplied nutrient for optimal burn wound healing and early recovery.

NCT ID: NCT00181974 Completed - Burns Clinical Trials

Efficacy of a Fibrin Sealant in Burn Surgery

Start date: March 2000
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of a fibrin glue in burn surgery with respect to hemostasis and skin graft fixation.

NCT ID: NCT00181753 Withdrawn - Burns Clinical Trials

Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition

Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to understand how the body uses amino acids in burned patients during the time they cannot eat normally. Amino acids occur naturally in the body and the food we eat. The body combines amino acids to make protein. It uses the proteins to do things such as heal wounds, fight infection, and provide energy. We are studying two ways of receiving nutrition: through a vein or through a tube. We are also studying two different types of food: with or without glutamine. The results of this study will be used to determine the best type and way to supply nutrients during a severe burn injury. We hope to learn how to help the body use nutrients more efficiently to better repair wounded tissues and recover earlier from injury.

NCT ID: NCT00161759 Completed - Burns Clinical Trials

Safety and Efficacy Study of Fibrin Sealant (FS 4IU) for Skin Graft Fixation and Wound Healing in Subjects With Burn Wounds

Start date: March 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess if Fibrin Sealant 4IU is as safe and efficacious as staples (the current standard of care) to achieve fixation of skin grafts and wound healing in subjects with burn wounds. Each subject receives staples as well as FS 4IU on comparable treatment sites.