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NCT ID: NCT02029261 Withdrawn - Burn Clinical Trials

Observational Study of Insulin Resistance and Muscle Wasting After Burn Injury

Start date: May 2014
Phase:
Study type: Observational

The purpose of this study is to examine important and significant problems, that of insulin resistance and muscle wasting after burn injury.

NCT ID: NCT01302457 Withdrawn - Burn Clinical Trials

Oral Care Study on Burn Patients

Start date: September 2007
Phase: N/A
Study type: Observational

There have been multiple articles done regarding oral hygiene on patients in burn and intensive care patients. All articles agree the need for good oral hygiene in these special needs patients. They also note that more research needs to be done on this subject, yet have no direction of how to proceed in this research. Currently, no research has been done on the burn/intensive care patient to see if there is a difference form the non-hospitalized patient which oral hygiene protocol is based on.

NCT ID: NCT01225107 Withdrawn - Burn Clinical Trials

Effect of Cranberry Extract on Infections in Burn Patients

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

Bacterial infections are a common complication in patients suffering from burns. These infections can cause significant morbidity and often mortality. Antimicrobial resistance coupled with the prevalence of burn-related infections warrants the identification of alternative substances in the treatment of burn-related infections. The cranberry has been examined as a potential agent in the prevention of other types of infections and it appears to have anti-adherence effects on bacteria. In addition, the cranberry has demonstrated general inhibitory effects against some types of bacteria suggesting that it may be a useful agent in the prevention of bacterial infections in burn patients. The purpose of the present study is to investigate the effect of cranberry extract on the incidence of infections in burn patients.

NCT ID: NCT00734695 Withdrawn - Burn Clinical Trials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: NCT00686478 Withdrawn - Burn Clinical Trials

Intron A for the Treatment of Hypertrophic Scar

Start date: n/a
Phase: Phase 3
Study type: Interventional

This study assesses the intervention with antifibrotic agents, specifically interferon (IFN) to reduce the magnitude and duration of hypertrophic scar. Burn patients with hypertrophic scar are randomly assigned to either an intervention IFN group or a placebo control group by subcutaneous injection three times a week. Patients are assessed using cutometer, mexameter, standardized photography, urinalysis, blood work, tissue biopsies and the Vancouver Burn Scar Assessment (VBSA) which rates selected HTS based on color, vascularity, height, pliability, itchiness and pain sensitivity. Once on treatment patients are assessed monthly for the six month treatment period.

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: 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: NCT00591916 Withdrawn - Burn Clinical Trials

New Treatment for Donor Sites

Donors
Start date: January 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Primary research questions/Purpose of the Research. 1. Determine the short term (epidermal regeneration, reduction of pain, infections and length of stay) and long term (scarring, long term recovery, and cost of treatment) outcomes of Microbial Nanocellulose (NC) and fine mesh gauze impregnated with hyaluronan and thrombin (HT). 2. Determine if donor site treatment with NC and HT is as safe as the use of Scarlet Red ointment dressing. b. Describe the importance of the knowledge that you expect to gain from the research. To find a donor site dressing that has outcomes equal or better than that of scarlet red.

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.