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Burns clinical trials

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NCT ID: NCT00796627 Terminated - Burns Clinical Trials

Hypoxia-inducible Factor-1 (HIF-1) Regulated Circulating Angiogenic Cells (CACs) Recruitment in Burn Wound Healing

Start date: December 2006
Phase: N/A
Study type: Interventional

This research is being done to increase knowledge about wound healing and different factors that may affect healing in burn patients.

NCT ID: NCT00794742 Completed - Burns Clinical Trials

Antimicrobial Resistance of Bacteria in Burn Patients

Start date: November 2008
Phase: N/A
Study type: Observational

The purpose of this study is to test the resistance of pathogenic bacteria in infected tissues of burn patients to various antimicrobials and enzyme debriders.

NCT ID: NCT00787592 Completed - Burns Clinical Trials

SSD vs Collagenase in Pediatric Burn Patients

Start date: January 2008
Phase:
Study type: Observational

The objective of this study is to evaluate the outcomes of children with burn injury with regard to the utilization of Silver sulfadiazine (SSD) cream and Collagenase ointment. The primary outcome variable will be need for skin grafting. The specific aim of the study is to prospectively collect data to determine if SSD is superior to Collagenase with regard to avoiding the need for skin grafting.

NCT ID: NCT00782054 Completed - Pruritus Clinical Trials

Evaluation of Post Burn Rehabilitation Population for Itch Control

Start date: September 2006
Phase: Phase 4
Study type: Interventional

Severe itching following burn injury is a common complication. As many as 87% of burn patients report severe itching. The intense itching can increase anxiety and can interfere with sleep and normal activities of daily living thus affecting quality of life. Often the itching will become so intense patients will scratch or rub the skin until an open wound develops. Current treatment for itching includes antihistamines, steroids. and/or moisturizers, but too often, the patient does not receive relief, even from drugs, and suffers undesirable side effects. Swiss-American Products, Inc, has developed a new skin moisturizer containing a blend of endopeptidase enzymes. These products have resolved itching in other types of skin disease such as dermatitis. The hypothesis that itching can be reduced through the use of these endopeptidase enzyme containing products in the post burn population will be tested.

NCT ID: NCT00774033 Terminated - Burn Clinical Trials

Epidermal Cells Delivery and Acute Burns

ENSEM
Start date: December 2008
Phase: Phase 3
Study type: Interventional

The aim of the study is to compare results obtained with epidermal cell spray and classic skin grafting for epidermal replacement in acute burns

NCT ID: NCT00734695 Withdrawn - Burn Clinical Trials

Comparing the Use of Vitamin c (Ascorbic Acid) in Eye Burn in Subconjunctival Injection to Topical or Oral Treatment.

Start date: July 2009
Phase: Phase 1
Study type: Interventional

Eye burns may cause a severe permanent damage. One kind of treatment is the use of vitamin C (Ascorbic acid). This study will compare between subconjunctival topical and/or systemic route of administration and topical and/or systemic administration.

NCT ID: NCT00732485 Withdrawn - Burn Clinical Trials

Mitochondrial Oxidation and Insulin Resistance in Burn Patients Treated With Fenofibrate

Start date: August 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Major burn injury causes significant insulin resistance on glucose and protein metabolism that persists for up to 6 months after the acute injury This project proposes to answer the following questions: 1. Will fenofibrate given to burn patients with insulin resistance restore their insulin sensitivity? 2. What is the relationship between mitochondrial dysfunction in muscle tissue as the causative mechanism of burn related insulin resistance? 3. To what extent will the restored insulin sensitivity affect glucose and protein metabolism in muscle, regenerating wounds and the liver, i.e. ameliorate burn related hyperglycemia and protein catabolism?

NCT ID: NCT00731887 Withdrawn - Burns Clinical Trials

Large Burn Outcome Study

LBO
Start date: June 2011
Phase: N/A
Study type: Observational

To examine long term physical and psychosocial outcomes of pediatric burn survivors. We want to learn about thoughts, feelings, coping style, social support, and overall adjustment following burn injury.

NCT ID: NCT00723008 Completed - Burns Clinical Trials

Cranial Electrotherapy Stimulation in Burned Patients

CES
Start date: May 2007
Phase: Phase 2
Study type: Interventional

To find out if Cranial Electrotherapy Stimulation is a useful treatment for people who have been burned and have Post Traumatic Stress Disorder. CES may be helpful in giving relief to some or all of those symptoms.

NCT ID: NCT00718978 Completed - Burns Clinical Trials

Clinical Application of Autologous Three-Cellular Cultured Skin Substitutes (CSS)

Start date: June 2003
Phase: N/A
Study type: Interventional

The aim of this work was to present the investigators experience in the use of autologous three-cellular cultured skin substitutes (CSS) consisting of cultured keratinocytes, melanocytes and fibroblasts attached to a scaffold of hyaluronic acid. This method represents a surgical alternative in the treatment of a variety of pathologies, including burns, ulcers and giant nevi.