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Wounds and Injuries clinical trials

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NCT ID: NCT03070938 Completed - Pressure Ulcer Clinical Trials

PuraPly™ Antimicrobial Wound Matrix and Wound Management

PuraPlyAM
Start date: November 2016
Phase: N/A
Study type: Observational

The PuraPly Antimicrobial Wound Matrix (PuraPly AM) case series is a prospective, observational study for patients who have received PuraPly AM which consists of a collagen sheet coated with polyhexamethylenbiguanide hydrochloride (PHMB) and is intended for the management of wounds; no experimental intervention is involved.

NCT ID: NCT03070925 Completed - Pressure Ulcers Clinical Trials

Prospective PuraPly™ AM Case Series Study

Start date: November 2016
Phase: N/A
Study type: Observational

The PuraPly AM case series is a prospective, observational study for patients who have received PuraPly AM which consists of a collagen sheet coated with polyhexamethylene biguanide hydrochloride (PHMB) and is intended for the management of wounds; no experimental intervention is involved.

NCT ID: NCT03069755 Completed - Trauma Clinical Trials

Perioperative Mortality Rate in Indian Trauma Patients

Start date: January 2017
Phase:
Study type: Observational

This study aims to estimate the perioperative mortality rate in adult trauma patients undergoing acute surgery as well as the association between type of acute surgery and perioperative mortality in university hospitals in urban India.

NCT ID: NCT03068104 Completed - Trauma Clinical Trials

Unmet Need for Massive Transfusion in Indian Trauma Patients

Start date: January 2017
Phase:
Study type: Observational

This study aims to estimate the difference between predicted and provided massive transfusion in adult trauma patients admitted to university hospitals in urban India.

NCT ID: NCT03063814 Completed - Clinical trials for Musculoskeletal Injury

Effects of App-based Versus Personal On-site Instruction on Neuromuscular Activity in Injury Prevention Exercises

ACL01
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

Therefore, the aim of the present study was to evaluate neuromuscular characteristics observed during a single bout of selected and validated injury preventive exercises instructed by an app (in accordance with 'Get set - Train smarter') versus gold standard instruction, supervision and feedback provided on-site by an expert. The present evaluation targets a population of female football and handball players without any previous exposure to injury prevention training.

NCT ID: NCT03061565 Completed - Clinical trials for Traumatic Brain Injury

Long Term Effects of Erythropoietin in Patients With Moderate to Severe Traumatic Brain Injury

Start date: August 1, 2017
Phase:
Study type: Observational

Traumatic brain injury is catastrophic event that commonly require treatment in an intensive care unit. Management is mainly supportive aiming at avoiding hypoxia, hypotension, hypoglycaemia and increased intracerebral pressure. Thus far efforts to find a specific pharmacologic therapies have been disappointing. Recently it was demonstrated that recombinant erythropoietin has been found to decrease mortality at six months from injury but without significantly improving functional neurological outcome (GOSe). Whether this survival benefit of EPO is sustained beyond 6 months is unknown. In the current study survival data will be collected centrally and patients alive or person responsible will be invited to participate in an evaluation of neurological function and quality of life. Factors associated with time to death as well as factors associated with long term quality of life will be determined with statistical methods.

NCT ID: NCT03056157 Completed - Clinical trials for Post-traumatic Stress Disorder

Psychosocial Rehabilitation After Moral Injury and Loss With Adaptive Disclosure

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

The aim of this study is to determine the efficacy of Adaptive Disclosure for Moral Injury and Loss (AD-MIL), a combat-specific psychotherapy for war-related PTSD stemming from Moral Injury (MI) and traumatic loss (TL) with Iraq and Afghanistan War Veterans with PTSD. AD-MIL will be compared to Present Centered Therapy (PCT). AD-MIL is a modified version of Adaptive Disclosure (AD), which has been modified and extended to solely treat MI and TL by targeting psychological and behavioral obstacles to occupational, relationship, and family functioning, as well as quality of life. PCT is a manualized evidenced-based PTSD treatment used in several large-scale PTSD trials. The primary end-point is psychosocial functioning (improvements in social, educational and occupational functions and improvements in quality of life). Secondary end-points include PTSD, depression, and shame and guilt. The investigators will also explore the impact of AD-MIL on anger and aggressive behaviors, suicidal ideation, and alcohol abuse.

NCT ID: NCT03050970 Completed - Head Trauma Clinical Trials

Infant Minor Head Trauma Clinical Decision Rule

PELICAN
Start date: February 11, 2017
Phase:
Study type: Observational

The purpose of this study is to validate a clinical decision rule for the management of minor head trauma in infants aged less than two years, constructed with the intention of minimizing the rate of computed tomography scans ordering.

NCT ID: NCT03050489 Completed - Clinical trials for Coronary Artery Disease

Assessment of Myocardial Ischemic-Reperfusion Injury During Off- and On- Pump CABG

Start date: September 15, 2015
Phase:
Study type: Observational

Assessment of myocardial ischemic-reperfusion injury during off- and on- pump CABG.

NCT ID: NCT03049150 Completed - Acute Kidney Injury Clinical Trials

PREdicting RENAL Injury In Patient After Hip Fracture Surgery

PRE-RENAL
Start date: February 3, 2017
Phase:
Study type: Observational

To determine whether MALDI, a type of Mass-Spectometry, can use protein pattern detection within urine to predict postoperative (after an operation) kidney damage in adults who have undergone emergency hip fracture surgery?