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Wounds and Injuries clinical trials

View clinical trials related to Wounds and Injuries.

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NCT ID: NCT01400607 Terminated - Clinical trials for Defect of Articular Cartilage

Neocartilage Implant to Treat Cartilage Lesions of the Knee

Start date: July 2011
Phase: Phase 3
Study type: Interventional

ISTO Technologies, Inc. is proposing a clinical study with 225 subjects, to establish the safety and efficacy of the Neocartilage Implant for the treatment of ICRS Grade 3 and 4 articular cartilage lesions of the knee compared to microfracture treatment.

NCT ID: NCT01382173 Terminated - Knee Osteoarthritis Clinical Trials

Monitoring Of Helsingborg Acute Knee Injuries (MOHAK)

Start date: March 2012
Phase:
Study type: Observational

Using magnetic resonance imaging (MRI), laboratory analyses and patient reported outcomes, the overall aim of this study is to investigate structural injuries and biochemical alterations in the acutely injured knee and to relate these findings to clinical outcomes at various time points.

NCT ID: NCT01328860 Terminated - Spinal Cord Injury Clinical Trials

Autologous Stem Cells for Spinal Cord Injury (SCI) in Children

Start date: April 2011
Phase: Phase 1
Study type: Interventional

The purpose of this research study is: 1. To see if Bone Marrow Cell harvest and transplantation are safe in children with Spinal Cord Injury, and 2. To determine if late functional outcome is improved following Bone Marrow Cell transplantation in children with Spinal Cord Injury, using pre-transplantation spinal cord function as the control.

NCT ID: NCT01325584 Terminated - Cancer Clinical Trials

Compassionate Use of Omegaven® in the Treatment of Parenteral Nutrition Induced Hepatic Injury

Start date: October 2012
Phase: Phase 2
Study type: Interventional

The purposes of this study are to make Omegaven® available to cancer patients with liver disease and to determine if Omegaven® can improve or prevent further liver disease. The study will also look at the effects Omegaven® has on immune function.

NCT ID: NCT01292811 Terminated - Spinal Cord Injury Clinical Trials

Restoration of Upper Limb Function in Individuals With Sub-Acute Spinal Cord Injury

MCRCT
Start date: January 2011
Phase: N/A
Study type: Interventional

The objective of this research program is to conduct a multi-site clinical randomized control trial that will evaluate the efficacy of functional electrical stimulation based upper limb intervention for people with tetraplegia. This will involve recruiting 84 persons with sub-acute tetraplegia across four sites (Montreal,Toronto, Fredericton and Edmonton) and will serve to evaluate three new Canadian hand function assessments that have been specifically developed for persons with tetraplegia. Although these assessments have been recently tested and have shown considerable promise, further evaluation on their clinical utility (in particular their responsiveness and validity) is required. As well, they need to be compared with one another to determine whether any of these tests is more appropriate for clinical applications or whether further test reduction or augmentation may be required. Having measures that are sensitive and accurate in assessing hand function is key for systematically evaluating emerging therapeutic interventions.

NCT ID: NCT01279369 Terminated - Pregnancy Related Clinical Trials

The Use of Fetal Fibronectin to Predict Delivery Due to Abruptio Placenta

Start date: October 2009
Phase:
Study type: Observational

The purpose of this study is to determine if the presence of fetal fibronectin in the cervicovaginal secretions of pregnant patients with minor maternal trauma predicts impending preterm delivery due to abruptio placenta.

NCT ID: NCT01275976 Terminated - Sepsis Clinical Trials

Effect of C1-esterase Inhibitor on Systemic Inflammation in Trauma Patients With a Femur or Pelvic Fracture

CAESAR
Start date: April 2012
Phase: Phase 3
Study type: Interventional

Trauma and major operation are associated with an excessive inflammation reaction due to tissue injury. This overwhelming immune response is considered to be a major risk factor in the pathogenesis of late inflammatory complications such as acute respiratory distress syndrome (ARDS), multiple organ dysfunction syndrome (MODS) and sepsis. The investigators hypothesize that administration of C1-esterase inhibitor (C1-INH) will attenuate the humane inflammatory response and, thereby, reduce the risk of inflammatory complications due to surgical interventions in trauma patients with a femur or pelvic fracture

NCT ID: NCT01217047 Terminated - Spinal Cord Injury Clinical Trials

Study on Functional Electrical Stimulation (FES) Cycling Following Spinal Cord Injury

CURE-SCI
Start date: October 2010
Phase: Phase 2/Phase 3
Study type: Interventional

This research is being done to study the effect of Functional Electrical Stimulation (FES) cycling on factors in blood and spinal cord in people with spinal cord injury (SCI).

NCT ID: NCT01201291 Terminated - Clinical trials for Traumatic Brain Injury | Patient

Impact of Inspired Oxygen Fraction on Outcome in Patients With Traumatic Brain Injury

BRAINOXY
Start date: November 2010
Phase: N/A
Study type: Interventional

Aim of the study is to investigate the impact of two different fractions of inspired oxygen (FiO2) on outcome in patients with severe traumatic brain injury (TBI).

NCT ID: NCT01191567 Terminated - Wounds Clinical Trials

Negative Pressure Wound Therapy. Therapy Effects and the Impact on the Patient's Quality of Life

Start date: September 2010
Phase: N/A
Study type: Interventional

Wounds have long been a source of suffering for unfortunate victims and in recent years new complementary methods have been developed in areas where traditional wound treatment has been insufficient. Treating wounds with negative pressure, Vacuum assisted closure® [VAC], is a relatively new method of treatment and knowledge about its effect on patients is limited. Earlier studies haven't been able to answer the question about which groups of patients that are in most favour of the treatment and what impact the treatment has on the patient's quality of life. It is important with further research since an effective and mild wound treatment can decrease suffering and increase quality of life for the patient. Wound treatment that does not lead to an achieved treatment goal can lead to a risk for the patient and should be avoided. The project consists of 4 part studies: Study 1 and 2 are chart review studies of a consecutive series of patients treated with VAC at Södersjukhuset during a 3 year period. The patients are described on the basis of medical, surgical and demographical factors. Outcome is treatment results and risk factors for a treatment failure. Study 3 and 4 are clinical randomised studies with the aim of studying whether treatment with VAC provides a faster and more effective healing of acute and postoperative wounds, and in what way the treatment affect the quality of life and pain of the patients, compared to conventional treatment.