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Wounds and Injuries clinical trials

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NCT ID: NCT03643419 Recruiting - Clinical trials for Spinal Cord Injuries

Clinical Study of Treatment of Acute Spinal Cord Injury by Near Infrared Light Irradiation

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

The purpose of this study was to observe the therapeutic effect of near-infrared light irradiation on the treatment of acute spinal cord injury in humans, and whether it can promote the recovery of neurological function. Half of the patients underwent laminectomy and decompression surgery, and the other half of the patients were implanted with irradiated fibers for irradiation after surgery.

NCT ID: NCT03635736 Recruiting - Clinical trials for Brain Injuries, Acute

Acustocerebrography (ACG) in Severe Brain Injury

ACG-BrainICU
Start date: August 14, 2018
Phase:
Study type: Observational

The study will enable the clinical applicability of the multiple-spectral-sonography for detection of severe brain injury in ICU patients. For this, the ACG diagnostic system (Sonovum AG, Leipzig, Germany) should be used as additional diagnostic tool in prospective single-center study.

NCT ID: NCT03629418 Recruiting - Acute Kidney Injury Clinical Trials

Targeted Blood-pressure Management and Acute Kidney Injury After Coronary Artery Bypass Surgery

Start date: August 14, 2018
Phase: N/A
Study type: Interventional

Acute renal injury (AKI) is a common complication after cardiac surgery and is associated with worse outcomes. It is now realized that intraoperative hypotension is an important risk factor for the development of AKI. In a recent randomized controlled trial of patients undergoing major noncardiac surgery, intraoperative individualized blood-pressure management reduced the incidence of postoperative organ dysfunction. The investigators hypothesize that, for patients undergoing off-pump CABG, targeted blood-pressure management during surgery may also reduce the incidence of postoperative AKI.

NCT ID: NCT03625193 Recruiting - Clinical trials for Spinal Cord Injuries

Psychometric Properties of Sit-to-stand Test in Spinal Cord Injury

Start date: October 1, 2017
Phase:
Study type: Observational [Patient Registry]

1. Do different arm placements (including arms on armrests/devices, arms on knees, arms free, and arm crossed over chest) influence outcomes of sit-to-stand test (STST) in ambulatory individuals with spinal cord injury (SCI)? 2. What are the factors associated with ability to perform STST in ambulatory individuals with SCI? 3. Are the single-time sit-to-stand test (STSST) and five-time sit-to-stand test (FTSST) reliable, valid and responsive to determine functional alteration in ambulatory individuals with SCI?

NCT ID: NCT03621254 Recruiting - Spinal Cord Injury Clinical Trials

Investigation Into Optimal FES Training Characteristics After Spinal Cord Injury

Start date: January 7, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to investigate two different modalities of functional electrical stimulation (FES) leg exercise in patients with spinal cord injury (SCI). The primary outcomes being compared are 1. FES-induced leg aerobic fitness, and 2. FES-induced leg strength. There will be two FES-leg training groups, and sub-acute patients with SCI will be randomised between the groups - high-short [HI-SHORT] and low-long [LO-LONG]. Both groups (n=10 per group) will exercise on the Hasomed RehaStimâ„¢ exercise ergometer for 6-8 weeks, three-four times per week (24 therapy sessions). [HI-SHORT] will perform 10 x 2-min of high-intensity interval training with a recovery of 1-2 min between exercise bouts. [LO-LONG] will perform 20+ min of continuous exercise at a low-moderate exercise intensity. Exercise intensity for [HI-SHORT] and [LO-LONG] will be titrated by neuromuscular stimulation characteristics. The primary outcomes will be assessed before training commences and after 6-8 weeks of training has been completed.

NCT ID: NCT03618940 Recruiting - Burn Injury Clinical Trials

Module on Preventing Fire, Burns and Scalds Injury Among Children

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

The main aim of this intervention study is to test the hypothesis if school based educational intervention program will significantly improve the knowledge of primary school student on childhood burn prevention in Kuala Lumpur. The secondary aim the evaluate the association of demographics background, burn injury history with knowledge on burn. The study was conducted in 12 primary school in Kuala Lumpur from 1st January 2015 to 31st December 2017 in three different phases.

NCT ID: NCT03608956 Recruiting - Acute Kidney Injury Clinical Trials

Renal Oxygen Saturation and Its Association With Acute Renal Injury

Start date: May 1, 2018
Phase:
Study type: Observational

Peri-operative renal dysfunction is a major mortality and morbidity cause following cardiac and major vascular surgery. Although several intra-operative strategies are proposed for better outcomes, no effective and fast resulting test is available to be done in operating rooms to assess renal functions. Urine and blood markers as serum creatinine, urine output, fractional excretion of sodium and urea are used for early diagnosis of acute renal injury. Near infrared spectroscopy (NIRS) assesses tissue oxygenation especially cerebral regional oxygen saturation. The benefit of NIRS followups of cerebral and somatic (liver, kidney, mesentery) oxygenation in pediatric cardiovascular surgery patients are demonstrated by studies.

NCT ID: NCT03598504 Recruiting - Clinical trials for Spinal Cord Injuries

Vibration for Muscle Spasms After Spinal Cord Injury

Start date: July 16, 2019
Phase: N/A
Study type: Interventional

This study uses closed-loop control of tendon vibration to implement clinically meaningful management of muscle spasms after spinal cord injury (SCI), and to understand the mechanisms responsible for spasm generation change in response to vibration.

NCT ID: NCT03598387 Recruiting - Acute Kidney Injury Clinical Trials

Automated Peritoneal Dialysis Versus Intermittent Hemodialysis in Acute Kidney Injury

SAFE-APD
Start date: April 24, 2018
Phase: N/A
Study type: Interventional

This is a multi-center randomized clinical trial study. The purpose of this study is to examine safety, feasibility and efficacy of automated peritoneal dialysis as compared with intermittent hemodialysis for AKI patients with indications for dialysis.

NCT ID: NCT03590028 Recruiting - Acute Kidney Injury Clinical Trials

An Early Real-Time Electronic Health Record Risk Algorithm for the Prevention and Treatment of Acute Kidney Injury

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

This is a single center randomized trial that seeks to determine if the use of an automated real-time electronic medical record Acute Kidney Injury (AKI) risk score can improve patient outcomes through the use of an early standardized nephrology focused intervention.