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NCT ID: NCT02381444 Completed - Clinical trials for Parkinson's Disease (PD)

Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Continuing Oral Therapy

BALANCE
Start date: April 17, 2015
Phase:
Study type: Observational

The aim of this study is to assess the effect of LCIG (levodopa-carbidopa intestinal gel) on HRQL (Health-Related Quality of Life) of participants and compare the Health-Related Quality of Life between participants continuing to levodopa-carbidopa intestinal gel treatments versus participants continuing on oral therapy for Parkinson's Disease.

NCT ID: NCT02379806 Completed - Clinical trials for Venous Thromboembolism

The SYMPTOMS - SYstematic Elderly Medical Patients Thromboprophylaxis: Efficacy on Symptomatic OutcoMeS - Study

SYMPTOMS
Start date: September 3, 2015
Phase: Phase 3
Study type: Interventional

Venous thromboembolism (VTE) is a frequent condition, affecting 1.8 per 1,000 people every year. Admission to hospital is one of the main risk factors for VTE, and could account for up to 20% of all VTE, making VTE prevention in admitted patients an appealing option to reduce VTE global burden. The landmark MEDENOX trial and others demonstrated the efficacy of low molecular weight heparins (LMWH) in reducing a composite outcome of symptomatic and asymptomatic events, the latter accounting for the vast majority of events. Publication of these trials led to the implementation of thromboprophylaxis policies in hospitals, which acceptance has been variable. More recently, the use of thromboprophylaxis has been challenged after the publication of 1) a negative trial that used 'death from any cause' as main outcome, 2) a systematic review showing the lack of a clear efficacy on the risk of pulmonary embolism or death, 3) negative trials using new oral anticoagulants, 4) the last version of the American College of Chest Physicians Guidelines, focusing on symptomatic events only, downgraded its recommendation for thromboprophylaxis in medical patients to a 1B recommendation, restricting its use to patients 'at increased risk of thrombosis' and recommending against the use of thromboprophylaxis in patients at low risk of thrombosis, patients bleeding or at high risk of bleeding. However, a limitation of this interpretation of the data is that in most trials, patients with screened asymptomatic events were treated with anticoagulants, preventing the occurrence of symptomatic events during follow-up. Moreover, subgroup analyses showed that elderly patients were at high risk of thrombosis in these trials, and that LMWH could be particularly efficient in this subgroup of patients. Conversely, their risk of bleeding is also higher than in younger patients and the current trials were not powered to detect a difference in the bleeding risk between groups. Finally, the diagnostic and therapeutic management of VTE is more challenging in the elderly. Therefore, we planned a randomized controlled trial on the efficacy of LMWH for the prevention of symptomatic VTE in elderly patients.

NCT ID: NCT02379104 Recruiting - Clinical trials for Blood Coagulation Disorders

ROTEM® Sigma Performance Evaluation - Method Comparison With Predicate Device and Reference Intervals

ROSI-EVA
Start date: October 2017
Phase: N/A
Study type: Observational

ROTEM® sigma is a new thromboelastometric coagulation analysis system. The new system is fully automated allowing for a simple and safe operation compared to its predecessor model ROTEM® delta. Method comparison of ROTEM® sigma with predecessor model ROTEM® delta) - confirmation of equality. Confirmation of reference intervals of the ROTEM® systems.

NCT ID: NCT02378168 Completed - Clinical trials for Heart Surgical Procedures

6-month Follow up After Sevoflurane Postconditioning

Start date: April 2014
Phase: N/A
Study type: Observational

Retrospective analysis of a 6-month follow up within a randomised controlled study in cardiac surgery with pharmacological postconditioning (sedation on intensive care unit with sevoflurane)

NCT ID: NCT02377245 Enrolling by invitation - Clinical trials for Arthritis, Juvenile Rheumatoid

Juvenile Inflammatory Rheumatism (JIR) Cohorte

JIR-cohorte
Start date: January 2014
Phase:
Study type: Observational [Patient Registry]

The investigators created a cohort of patients with juvenile inflammatory rheumatisms with the purpose to follow them prospectively, and investigate the tolerance and efficacy of immunosuppresive and biological agents.

NCT ID: NCT02377180 Completed - Healthy Clinical Trials

Capsaicin-induced Muscle Pain in Humans

Start date: September 2014
Phase: N/A
Study type: Interventional

There is currently no specific diagnostic test for primary muscular pain. The present study investigates whether selective blockade of the suprascapular nerve can effectively abolish experimental pain arising from the supraspinatus muscle. Experimental muscle pain is induced by intramuscular injection of capsaicin, an alkaloid from red chili peppers. The study consists of three parts: 1. to describe the development, time course and intensity of capsaicin-induced muscle pain 2. to evaluate the effectiveness of suprascapular nerve block against capsaicin-induced muscle pain 3. to compare suprascapular nerve block and direct intramuscular local anesthetic infiltration for their effectiveness in capsaicin-induced muscle pain

NCT ID: NCT02377115 Completed - Clinical trials for Postoperative Delirium

Risk Assessment for Postoperative Delirium

RAPID
Start date: March 2015
Phase: N/A
Study type: Interventional

Postoperative delirium (POD) - a temporary state of confusion - is a frequent complication of surgery, which most commonly occurs in elderly patients. A tablet computer application that may assist preoperative risk screening for POD was developed at the University Hospital Basel in 2014. This study aims to investigate whether the computer program may assess the risk of a patient to develop POD.

NCT ID: NCT02376686 Completed - Depression Clinical Trials

Music Intervention in the Treatment of Sleep Disorders for Depressed Patients

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether music hearing in the evening before going to sleep can improve sleep quality, depressive symptoms and quality of life in patients with affective disorders.

NCT ID: NCT02375438 Completed - Clinical trials for Mitochondrial Diseases

Nutritional Assessment in Mitochondrial Cytopathy

NAMITO
Start date: December 2014
Phase: N/A
Study type: Observational

The aim of this study is to assess nutritional intake (quantitatively and qualitatively), nutritional state and body composition of patients suffering from mitochondrial cytopathy, compared to healthy controls. The energy intake will be calculated through dietary protocols, the energy expenditure by indirect calorimetry and body composition will be performed with bio-impedance analysis. Further on, the investigators expect to be able to provide nutritional counselling to this population in order to increase energy and protein intake, which may improve health and well-being.

NCT ID: NCT02375269 Not yet recruiting - Clinical trials for Postoperative Complication

Effect of Remote Ischemic Preconditioning on Postoperative Complications in Visceral Surgery

RIPC
Start date: March 2015
Phase: N/A
Study type: Interventional

Remote Ischemic Preconditioning (RIPC) is mediated by intermittent brief episodes (5-10 minutes) of short ischemia in a limb (i.e. arm), followed by reperfusion. For this purpose in 3-4 cycles, a tourniquet is insufflated to suprasystolic pressure levels for 5 minutes and deflated for 5 minutes afterwards. The ischemic episodes are known to stimulate platelets and factors platelet dependent factors such as Serotonin and VEGF. These humoral factors have a systemic effect and have the potential to protect target organs (i.e. heart, kidney, liver) remote to the ischemic limb. The purpose of this randomized controlled study is to investigate the influence and impact of RIPC on postoperative complications in patients undergoing visceral surgery