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Burns clinical trials

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NCT ID: NCT00734695 Withdrawn - Burn Clinical Trials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NCT ID: NCT00732485 Withdrawn - Burn Clinical Trials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NCT ID: NCT00731887 Withdrawn - Burns Clinical Trials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NCT ID: NCT00701623 Withdrawn - Burns Clinical Trials

Sodic Heparin Effectiveness of the Treatment of Burns

Heparin
Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Burns are injuries caused by agents thermal, chemical, electrical or radioactive who act in the tissue lining of the human body and may partially or totally destroy the skin and its annexes, to the deeper layers, as subcutaneous tissue, muscles, tendons and bones . Studies show that topical heparin has, in addition to the already known anticoagulant activity, anti-inflammatory properties, analgesic, and neoangiogenic, stimulating blood flow and increasing the repair of the fabric as well as the restoration of collagen and reepiteliztion. Moreover, the use of heparin reduces the need for painful medical procedures, as debridations, surgeries and transplants The intention of this work is to verify the effectiveness and safety of sodium heparin in the treatment of burns of the skin.

NCT ID: NCT00675974 Withdrawn - Burns Clinical Trials

Use of Pressure Garments for Burn Scars

Jobst
Start date: August 2005
Phase: Phase 2/Phase 3
Study type: Interventional

1. Will Pressure Garment Therapy better control hypertrophic scarring than no Pressure Garment Therapy. 2. How will Pressure Garment Therapy affect functional capacity or scar contracture development across joints either in number or severity. 3. Will Pressure Garment Therapy diminish discomfort due to pruritus.

NCT ID: NCT00674999 Withdrawn - Burn Clinical Trials

Use of Amnion on Partial Thickness Burns

Amnion
Start date: June 2005
Phase: Phase 2/Phase 3
Study type: Interventional

To determine if Amnion, used on partial thickness burn injuries would provide an improvement in rate of healing, pain control and scarring as compared to standard medical treatments.

NCT ID: NCT00643357 Withdrawn - Burns Clinical Trials

Study of the Efficacy and Safety of Kalinox® 170 Bar for the Performance of Care Procedures in Children With Burns

Burns
Start date: March 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and the safety of Kalinox® 170 bar, over a period of three consecutive care procedures in burned children. It's a international (Spain, France, Tunisia and Belgium) study with 8 investigator centers.

NCT ID: NCT00609661 Withdrawn - Wound Healing Clinical Trials

Adult Stem Cell Response to Burn Injury

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

This study is designed to determine the response of adult stems cells, also referred to as mesenchymal stem cells (MSCs), to tissue injury resulting from thermal burns. The study will consist of a one time collection of a patient's blood, about one teaspoon, on the third day following the initial burn. MSCs in the blood will then be quantitated and identified using according to unique proteins found on their cell surface using flow cytometry. The results of flow cytometry analysis will then be compared to the patients characteristics (age, sex, race, etc.), their past medical history (hx of diabetes, hypertension, heart disease, etc.) and to the patient outcome (length of hospital stay, mortality, etc.).

NCT ID: NCT00591604 Withdrawn - Burn Clinical Trials

High-Dose Vitamin D Deficiency in Burn Injury

VitaminD
Start date: February 2007
Phase: Phase 3
Study type: Interventional

High dose Vitamin D (50,000IU) therapy may increase bone mineral density/bone mineral content after large burns.

NCT ID: NCT00539019 Withdrawn - Burns Clinical Trials

Quantification and Derivation of Metabolic Needs in Children During Burn Rehabilitation

Start date: October 2006
Phase: N/A
Study type: Observational

The investigators are collecting information on the calorie needs of patients in the first year postburn. The investigators hypothesize that increased energy needs continue for up to a year following wound closure from burn injury.