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Burns clinical trials

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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: 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: 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: NCT04138355 Completed - Hand Burn Clinical Trials

The Clinical Utility of Extracorporeal Shock Wave Therapy on Hand Burns

Start date: November 2, 2019
Phase: N/A
Study type: Interventional

No study has investigated the effect of extracorporeal shock wave therapy (ESWT) on hand function and hypertrophic scar characteristics. To investigate ESWT effects on burned hands, the investigators compare the results of ESWT combined with manual therapy group to the results of matched conventional(CON) rehabilitation combined with manual therapy group.

NCT ID: NCT04136691 Completed - Burns Clinical Trials

The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning

Start date: February 19, 2018
Phase: N/A
Study type: Interventional

Aim: This research was conducted as a single-blind randomized control group intervention trial to determine the effectiveness of simulation method performed using high-fidelity human patient simulator in nursing students' burn patient care planning.

NCT ID: NCT04124133 Completed - Clinical trials for Second-degree Burn of Children

Evaluation of Efficacy and Safety of Ialuset Cream and Gauze in Second-degree Burns on Child

Start date: December 10, 2018
Phase:
Study type: Observational

Observational retrospective monocentric study occured in the univeristy hospital center of Bensançon the department of pediatric surgery. Data of patients treated in the hospital between January 2016 and January 2019 have been collected.

NCT ID: NCT04079998 Completed - Clinical trials for Trauma-related Wound

Procellera® Compared to Standard of Care Treatment in Mitigating Biofilm Formation in Acute Trauma and Burn Wounds

Start date: February 28, 2019
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate Procellera® , a novel FDA approved antimicrobial wound dressing in a prospective, randomized, controlled clinical study. The hypothesis is that when the dressing is moistened, the low electric field created by moisture-activated elemental silver and zinc electro-couple will prevent formation of biofilm in wounds or to disrupt existing biofilm.

NCT ID: NCT04073030 Completed - Burns Clinical Trials

Burn Injury In a Child Due to Cyanoacrylate-Based Nail Glue- Case Report and Literature Review

Cyanoacrylate
Start date: June 1, 2019
Phase:
Study type: Observational

Cyanoacrylate is used in the manufacturing of surgical adhesives, nail glue and super glue. After contact with cotton or wool, among other substances, a reaction is ignited, inflicting thermal damage to the skin underlying clothes. Nine papers have been published about such an incidence, majority of which involve children. In this paper, a four-year-old girl suffering from mixed-first-and-second degree burns due to cyanoacrylate spillage over the digits, anterior aspect of the right thigh and a patch of the skin on the left upper abdomen, spanning 4% of the total body surface area. The clothes were forcefully removed by the mother and shampoo was applied over the area. In the ER, irrigation with normal saline was done followed by dressing with paraffin- impregnated gauzes and silver sulfadiazine. Volar slabs were placed on the hands. The dressing in the hands was later changed to fusidic acid as the burn healed. Silicone sheet dressing was initiated twenty-eight days later after complete healing of the burned skin. An experiment conducted by the authors showed no difference in the pH of different cyanoacrylate products. The pH was not changed after applying shampoo over the nail glue immersed dip-stick. This paper aims to improve awareness about proper first-aid management which predicts the quality of the outcome. Further emphasis is required on providing a safe environment for the children and clear, comprehendible warning of hazards on the label of the cyanoacrylate based-products.

NCT ID: NCT04034849 Completed - Clinical trials for Burning Mouth Syndrome

Effects of Photobiomodulation in Burning Mouth Syndrome

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The main objective of this study is to assess the effects of Photobiomodulation with Low-level Laser Therapy to the pain management in Burning Mouth Syndrome patients, besides assessing their impact on the different aspects of their quality of life, using the necessary questionnaires to evaluate all the outcomes of chronic pain.