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Burns clinical trials

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NCT ID: NCT01268189 Completed - Burns Clinical Trials

Evaluation of Oxygen Diffusion Dressing for Accelerating Healing of Donor Site and Other Wounds

Start date: August 2010
Phase: N/A
Study type: Interventional

This is a single-center, prospective, randomized, and controlled study to evaluate the effectiveness of OxyBand Dressing for the use as a dressing for autogenous skin donor sites compared to our current standard donor site dressing (Xeroform). Hypothesis is that the mean healing time for wounds treated with the OxyBand dressing will be less than the mean healing time for wounds treated with the Xeroform dressing.

NCT ID: NCT01265056 Completed - Pain Clinical Trials

The Effect of Neurontin on Pain Management in the Acutely Burned Patient

Start date: February 2010
Phase: N/A
Study type: Interventional

Burn patients have extreme pain. Opioids are the main agents used for analgesia. We therefore propose a single center study to fruther assess the efficacy of neuropathic agents in controlling the pain associated with acute thermal injury.

NCT ID: NCT01254357 Completed - Trauma Clinical Trials

Burn Outcomes in Young Adult Burn Survivors

YA
Start date: December 2011
Phase: N/A
Study type: Observational

As part of Clinical Trials.Gov ID:NCT00253292 a psychometrically sound outcomes instrument was developed to study the outcomes of burn survivors in the 19-30 year old age group. This workgroup has come together to re-examine the data collected during the previous study and determine next steps in understanding the recovery for this population.

NCT ID: NCT01242423 Completed - Clinical trials for Burn Wound and Skin Graft Healing

Healing of Burns and the Effect of Shockwave Therapy on the Recovery of Skin Grafts

Start date: November 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The study is to review whether musculoskeletal shockwave therapy (ESWT) can speed up the healing of second-degree burns as well as skin-graft donor sites. In both cases, the primary hypothesis is the shortened period leading up to the complete healing of the wound (reepithelization). The secondary hypothesis in the course of the study assesses: the rare manifestation of undesirable local events (e.g. reddening, swelling, hematoma).

NCT ID: NCT01237964 Not yet recruiting - Clinical trials for Burn's Associated Contracture

Injectable Collagenase For Burns' Associated Contracture

Start date: March 2011
Phase: Phase 2
Study type: Interventional

A pilot experiment to test the efficiency of the enzyme Collagenase in treating contractures which result's from burn's healing process. So far, treatment of choice in patients with burn's created movement limiting contractures, concentrated around supportive care. Patients were referred to surgical intervention only if necessary. Treatment by injecting an external enzyme is avant-garde and hasn't been done under such conditions. This study might introduce a new kind of treatment, which can be done in ambulatory environment .This type of treatment might significantly improve patients' function and quality of life, with no need for a surgical intervention.

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: NCT01214980 Completed - Trauma Clinical Trials

Split Thickness Donor Site Healing With MIST Study

Start date: February 2012
Phase: N/A
Study type: Interventional

Subjects requiring skin grafting due to burns, trauma, or chronic venous ulcers with split thickness donor sites expected to be between 20 and 200 square cm will be consecutively screened for study eligibility. This study is a prospective, randomized, controlled trial evaluating effect of MIST Therapy on the healing of split thickness skin graft donor sites compared to standard care. Subjects meeting all eligibility criteria and providing appropriate written informed consent will be enrolled for study participation.

NCT ID: NCT01214811 Completed - Inflammation Clinical Trials

Open Multi-centre Investigation to Evaluate Signs and Symptoms of Local Inflammation/Infection on Chronic Ulcers and Partial Thickness Burns When Using Mepilex Border Ag as an Anti-microbial Wound Dressing

Start date: September 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the change in signs of inflammation/local infection when Mepilex Border Ag is used in normal clinical practice when used on chronic ulcers (venous leg, diabetic foot and pressure ulcers) and partial thickness burns in need* of topical antimicrobial treatment according to the physician.

NCT ID: NCT01213914 Active, not recruiting - Burns Clinical Trials

Hemofiltration in Burns: RESCUE (Randomized Controlled Evaluation of Hemofiltration in Adult Burn Patients With Septic Shock and Acute Renal Failure)

RESCUE
Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is determine if High-Volume Hemofiltration in addition to 'contemporary' care will result in an improvement of select clinical outcomes when compared to 'contemporary' care alone in the treatment of critically ill patients with ARF secondary to septic shock.

NCT ID: NCT01184547 Completed - Quality of Life Clinical Trials

Effects of a Community Based Exercise Program in Adults With Severe Burns

COMBEX
Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this proposal is to assess the efficacy of implementing a 12-week structured and supervised community-based exercise program (COMBEX) at hospital discharge. The investigators will assess the effect of exercise on mental health and physical function, along with its effects on the amelioration of the burn-induced catabolic response. The central hypothesis of this proposal is that exercise-induced physical and psychosocial benefits obtained during a supervised and structured COMBEX program in severely burned adults will improve physical function, and quality of life relative to Standard of Care (SOC).