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Second-degree Burn clinical trials

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NCT ID: NCT03530150 Completed - Second-degree Burn Clinical Trials

Pirfenidone and Its Role in Burn Wound Healing

Start date: January 1, 2017
Phase: Phase 2
Study type: Interventional

Burn patients which skin has been lost a rapid growth of the skin is a foremost in their treatment. Due to the injury, burn patients undergo a systemic inflammation that helps the skin heal faster. However, several studies have shown that this inflammation increases the levels of several inflammatory molecules that impairs skin growing, which further delays the recovery of burn patients. As such, by inhibiting these inflammatory molecules with the administration of a medication called pirfenidone burn patients might present faster rates of skin growth and recovery. Thus, patients suffering from a burn injury will be recruited at the emergency department of the Hospital University in Monterrey Mexico. Afterward, patients will be randomized to either receive pirfenidone 600 mg orally once per day or usual care consisting of covering the wound with hydrocolloid dressings. To assess the amount of newly growth skin investigators will take a small piece of the skin to further evaluate it through a microscope.

NCT ID: NCT02108535 Completed - Second-degree Burn Clinical Trials

Comparative Analysis of Cost-effectiveness of Silver Dressing in Burns

ARGENTUM
Start date: November 2013
Phase: Phase 4
Study type: Interventional

The evidence is insufficient to determine whether the types of dressings containing silver differ in time / proportion for complete wound healing and pain. We will analyze the cost-effectiveness of these dressings in outpatients, considering the service provided by the Brazilian National Public Health System.

NCT ID: NCT01055587 Completed - Second Degree Burn Clinical Trials

Diagnostic of Infections Following Major Abdominal Surgery and Burn Injury

Earlygnost
Start date: September 2009
Phase: N/A
Study type: Observational

This study was designed to investigate, if new biomarkers may improve the early diagnostic of infections following major abdominal surgery and severe burn injuries.

NCT ID: NCT00742183 Completed - Second Degree Burn Clinical Trials

Evaluating the Cost-effectiveness, Efficacy, Safety and Tolerance of Mepilex® Ag Versus Silvadene®

Start date: August 2008
Phase: N/A
Study type: Interventional

The primary objective is to compare the incremental costs (direct and indirect) and benefits (healing outcomes, quality of life) of using foam silver dressing (Mepilex® Ag) to a Silver sulfadiazine 1% cream (Silvadene®) from the perspective of the health care provider. The secondary objectives are to investigate the safety, the tolerance and the performance on burn status including pain.