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Burns clinical trials

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NCT ID: NCT04203134 Completed - Clinical trials for Burning Mouth Syndrome

Burning Mouth Syndrome Mouth Guard Prospective Study

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

This study will seek to test the effectiveness of a nonpharmacologic therapy for burning mouth syndrome (BMS). This nonpharmacologic therapy approach will be the fabrication a protective acrylic mouthguard for the maxillary arch and palate.

NCT ID: NCT04202289 Completed - Burns Clinical Trials

Use of Nile Tilapia Fish Skin as a Xenograft for Burn Treatment: Phase III Study

Start date: April 3, 2017
Phase: Phase 3
Study type: Interventional

The present study is a Phase III Randomized Clinical Trial aiming to evaluate the efficacy of Nile tilapia (Oreochromis niloticus) skin as an occlusive biological dressing in the treatment of superficial partial-thickness burns in adults.

NCT ID: NCT04200053 Completed - Burn Degree Second Clinical Trials

The Effect of Reflexology Massage and Passive Music Therapy Intervention Before Burn Dressing

Start date: August 12, 2019
Phase: N/A
Study type: Interventional

Reflexology massage applied before burn dressing reduces pain, anxiety and sleep problems

NCT ID: NCT04195126 Not yet recruiting - Burns Clinical Trials

Early Haemadsorption in Major Burns

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Major deep burns (>20% body surface, involving deep skin layers) and associated severe inflammatory reaction and their complication are one of the biggest challenge of intensive care. Haemoadsorption therapy, including the CytoSorb treatment is a promising novel therapeutic approach, but only case-studies are available in the literature yet. Based on data from septic shock patient treatment the investigators hypothesize that CytoSorb is beneficial in early treatment of burns. The investigators aim to conduct a randomised-controlled study to assess the clinical effectiveness (based on score systems including MODS, SOFA, APACHE II, KDIGO, ABSI), 7 and 28 days survival, intensive care length of stay, length of mechanical ventilation, resuscitation fluid need and ino/vasopressor drug doses and the presence and severity of organ dysfunctions, particularly renal dysfunction. The investigatora plan to conduct basic research to elucidate the pathophysiological background of clinical effect, including the measurement of inflammatory and anti-inflammatory cytokines, presence and severity of oxidative stress (lipid peroxidation, protein oxidation, reduced/oxidised glutathion levels) and organ dysfunction markers (kidney injury molecule -1, neutrophil gelatinase-associated lipocalin, cystatin-C, uromodulin).

NCT ID: NCT04192942 Not yet recruiting - Burns Clinical Trials

Protocol of Management of Major Pediatric Burn in Intensive Care Unit

Start date: December 2019
Phase: N/A
Study type: Interventional

Decrease mortality and morbidity in major pediatric burns

NCT ID: NCT04189367 Not yet recruiting - Clinical trials for Burning Mouth Syndrome

Treatment of Burning Mouth Syndrome With Integration of Traditional Chinese Medicine and Western Medicine

Start date: June 20, 2020
Phase: Phase 3
Study type: Interventional

This study is an open-label randomized controlled trial of the efficacy of the integration of Traditional Chinese medicine (TCM) and western medicine based on TCM syndrome differentiation. The hypothesis is (1) TCM model can identify the primary and secondary type burning mouth syndrome (BMS); (2) TCM model can identify BMS after treatment with western medicine; (3) There is a positive effect of TCM in treating BMS.

NCT ID: NCT04187586 Completed - Burn Scar Clinical Trials

Effect of Extracorporeal Shock Wave Therapy for Burn Scar Charateristics

Start date: December 10, 2019
Phase:
Study type: Observational

No study has investigated the effect of extracorporeal shock wave therapy (ESWT) on hypertrophic scar characteristics. Thus, this study aimed to ascertain the effects ESWT on burn scars. The investigators retrospectively reviewed burn patients who had undergone autologous split-thickness skin grafting (STSG) with same artificial dermis between January 2012 and September 2019.

NCT ID: NCT04162639 Withdrawn - Burns Clinical Trials

The Relationship Between Cadaveric Allograft Skin and HLA-Sensitivity in Burn Patients

Start date: February 2021
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to look at how the body's immune system reacts to temporary skin grafts from deceased donors.

NCT ID: NCT04157504 Completed - Burns Clinical Trials

Evaluation of Physical Functions in Lower Limb Burn Injury

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

This study evaluates scar tissue, normal range of motion of lowr extremity joints, lower extremity functions, functional capacity, functional mobility, kinesiophobia and quality of life in lower limb burn injury.

NCT ID: NCT04152096 Recruiting - Burns Clinical Trials

Efficacy and Safety of Rheosorbilact® Solution for Infusion, in a Complex Therapy of Burns

Start date: January 24, 2017
Phase: Phase 4
Study type: Interventional

This study evaluates the efficacy and safety of Rheosorbilact®, solution for infusion ("Yuria-Pharm" LLC), in comparison with Ringer's Lactate, solution for infusion, in a complex therapy of burns. Half of participants will receive Rheosorbilact® in complex therapy, while the other half will receive Ringer's Lactate in complex therapy.