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NCT ID: NCT01470950 Active, not recruiting - Clinical trials for Spinal Cord Injuries

Characterization of the Changes in the Signalling Pathways During Spinal Cord Injury-induced Skeletal Muscle Atrophy

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

Atrogin-1 and muscle RING finger-1 are skeletal muscle specific genes, with ubiquitin ligase activities, that are upregulated during muscle atrophy in mice. The Akt/GSK3 and Akt/mTOR pathways are involved in muscle hypertrophy in mice. Recent studies by the investigators team and others have demonstrated the implication of these signalling pathways in the control of muscle mass in humans. However no study has yet investigated the involvement of these systems in the early stages of spinal cord injury induced human skeletal muscle atrophy. The investigators propose to investigate the level of expression of the different components of the ubiquitin-proteasome system together with the level of expression and activity of the Akt/mTOR and Akt/GSK3 signalling pathways after SCI in humans during the first months following the injury. A second aim of this project is to assess if a novel apparatus of electrical stimulation which generate movements by closed-loop electrical muscle stimulation may improve strength and muscle mass in these patients. The patients will be recruited jointly at the Clinique Romande de Réadaptation (CRR) in Sion and the Swiss paraplegic centre in Nottwil. They will be randomly divided into two groups, a first group of patients will undergo a conventional treatment of rehabilitation while a second set of patients will be treated using a brand new system of electro-stimulation called MotionMaker TM. Biopsies will be obtained in the first weeks after admission; two other biopsies will be taken respectively 3 and 6 months post-lesion. Our results will provide an increased understanding of the molecular mechanisms contributing to skeletal muscle atrophy during the early stages following SCI and a characterization of the impact of endurance training in the no more voluntary innervated muscle. Moreover this study will also investigate the potential improvement in the rehabilitation process by using a new system of electro-stimulation.

NCT ID: NCT01470014 Completed - Clinical trials for Left Ventricular Noncompaction

Cardiac Computed Tomography: Characteristics of Isolated Left Ventricular Non-compaction

Start date: October 2011
Phase: N/A
Study type: Observational

The diagnostic criteria for isolated left ventricular non-compaction cardiomyopathy (IVNC) have been well established for echocardiography and cardiac magnetic resonance, such validation is lacking for computed tomography (CT). Such criteria are of great clinical relevance as a growing number of patients undergo a cardiac CT scan in daily clinical routine. The investigators aim to test the diagnostic accuracy of cardiac CT in distinguishing IVNC from lesser degrees of trabecular layering seen in potential differential diagnoses such as cardiomyopathies and left ventricular hypertrophy or dilation. The investigators hypothesize that echocardiographic diagnosed pathological trabeculation can be distinguished by determining the ratio of non-compacted to compacted myocardium on cardiac CT.

NCT ID: NCT01467739 Completed - Clinical trials for Endotracheal Intubation

Evaluation of the Ambu ® aScope® for Tracheal Intubation in Difficult Airways

Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a disposable fiberscope (Ambu ® aScope®) for tracheal intubation in difficult airways due to cervical immobilization by a cervical collar, and compare it to a conventional reusable fiberscope.

NCT ID: NCT01467453 Enrolling by invitation - Glaucoma Clinical Trials

Clinical Application of Sensimed Triggerfish Sensor (TS) With Wireless Signal Transmission for Continuous Intraocular Pressure Measurement

Start date: November 2011
Phase: Phase 4
Study type: Observational

The study objective is to investigate the clinical applicability of continuous IOP measurement using TS with radio transmission over 24 hours. - Trial with medical device

NCT ID: NCT01467440 Enrolling by invitation - Glaucoma Clinical Trials

Efficacy of Selective Laser Trabeculoplasty in Patients Under Treatment With Topical Prostaglandines

Start date: November 2011
Phase: Phase 4
Study type: Observational

Retrospective analysis of efficacy of selective laser trabeculoplasty in patients under treatment with topical prostaglandins compared to patients without topical prostaglandins is performed. Inclusion criterion are patients with glaucoma or ocular hypertension, who underwent treatment with selective laser trabeculoplasty due to insufficient control of intraocular pressure during their routine treatment at the University Hospital Zurich / Division of Ophthalmology.

NCT ID: NCT01467388 Enrolling by invitation - Glaucoma Clinical Trials

Efficacy of Selective Laser Trabeculoplasty in Pseudophakic Patients

Start date: November 2011
Phase: N/A
Study type: Observational

Retrospective analysis of efficacy of selective laser trabeculoplasty in pseudophakic patients compared to phakic patients is performed. Inclusion criterion are patients with glaucoma or ocular hypertension who underwent treatment with selective laser trabeculoplasty due to insufficient control of intraocular pressure during their routine treatment at the University Hospital Zurich / Division of Ophthalmology.

NCT ID: NCT01467323 Completed - Clinical trials for Diabetes Mellitus, Type 2

Efficacy and Safety of Biphasic Insulin Aspart 30 in Type 1 or Type 2 Diabetes

Start date: April 1998
Phase: Phase 3
Study type: Interventional

This trial is conducted in Europe. The aim of this trial is to evaluate the efficacy and safety of biphasic insulin aspart 30 in subjects with type 1 or type 2 diabetes.

NCT ID: NCT01467193 Completed - Insulin Sensitivity Clinical Trials

The Effect of Dietary Fat Load and Physical Exercise on the Flexibility and Partitioning of Ectopic Lipids.

Start date: August 2011
Phase:
Study type: Observational

This study aims at assessing the effect of standardized dietary fat load and short-term aerobic exercise on systemic lipolysis, flexibility and partitioning of ectopic fat stores (intramyocellular = IMCL, intrahepatocellular = IHCL, intramyocardial lipids = IMCaL) in relation to FFA in endurance trained athletes and hypopituitary patients compared to sedentary healthy control subjects. Exercise is a powerful stimulation for growth hormone (GH) secretion in health. A standardised exercise test can, therefore, be discriminative for the diagnosis of GH-deficiency in adults. This will be assessed. Hypothesis (ectopic fat stores) 1. Ectopic fats stores are flexible fuel stores and are influenced by diet and physical activity.FFA availability may play an important regulatory role. 2. There is a tissue specific partitioning of triglycerides and/or FFA among non-adipose organs after fat load and physical exercise 3. The flexibility of ectopic fat stores is related to insulin sensitivity 4. Lipolytic and anti-lipolytic hormones are critical for regulating FFA availability (at rest or during exercise) and therefore also for the regulation of ectopic fat stores. 5. GH is a lipolytica hormone. Lack of GH in adulthood is related to decreased FFA availability thereby influencing ectopic lipid stores Hypothesis diagnosis of GHD 6. A short intensive physical exercise shows a good discriminative power to diagnose GHD.

NCT ID: NCT01467167 Completed - Anesthesia,General Clinical Trials

Utility of the Smart Pilot View in Clinical Practice: A Two Center Prospective Observational Study

Start date: October 2011
Phase:
Study type: Observational

Recently, a new software program for anesthesia has been developed, called Smart Pilot View. This program monitors the patient, the anesthetic drugs given, and the calculated depth of the anesthesia. The purpose of this study is to determine whether the use of this program improves the quality of anesthesia.

NCT ID: NCT01467102 Completed - Clinical trials for Chronic Postoperative Pain

euCPSP: European Observational Study on Chronic Post Surgical Pain,PAIN-OUT Study

PAIN-OUT
Start date: July 2011
Phase: N/A
Study type: Observational

This project a European observational study on the incidence and characteristics of chronic post surgical pain (CPSP). Research Questions - What is the incidence of chronic post surgical pain (CPSP) in Europe? - What are the risk factors of chronic post surgical pain (CPSP) related to surgery, patient and anaesthesia management? - What are the difference in incidence and risk factors in different European countries?