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NCT ID: NCT02596152 Completed - Obesity Clinical Trials

Mini-trampoline Intervention vs. Nordic Walking: Balance, Fitness and Neuropsychological Effects

TraWaFit
Start date: August 2015
Phase: N/A
Study type: Interventional

The effects of mini-trampoline training on balance, cardiorespiratory fitness, strength and neuropsychological parameters in an overweight or obese population are unknown. The aim of this 2-arm randomized controlled trial is to compare the effects of a 12-week mini-trampoline training and a 12-week nordic walking training on balance, fitness and strength in overweight/obese individuals.

NCT ID: NCT02595814 Terminated - Acute Heart Failure Clinical Trials

Global Non-interventional Heart Failure Disease Registry

REPORT-HF
Start date: July 23, 2014
Phase:
Study type: Observational [Patient Registry]

The clinical characteristics, initial presentation, management, and outcomes of patients hospitalized with new-onset (first diagnosis) heart failure (HF) or decompensation of chronic HF are poorly understood worldwide. REPORT-HF is a global, prospective, and observational HF disease registry designed to characterize patient trajectories longitudinally during and following an index hospitalization for acute HF.

NCT ID: NCT02595632 Completed - Healthy Subjects Clinical Trials

Breath Analysis in Healthy Controls

Start date: November 2015
Phase:
Study type: Observational

The purpose of this study is to detect a specific profile of breath in healthy subjects by an untargeted metabolomic study using exhaled breath analysis by mass spectrometry.

NCT ID: NCT02595411 Completed - Stroke Clinical Trials

Reliability of the Melbourne Assessment

Start date: July 2015
Phase: N/A
Study type: Observational

The aim of the study is to investigate the reliability of the Melbourne Assessment.

NCT ID: NCT02594501 Active, not recruiting - Angina, Unstable Clinical Trials

Randomized Trial of COBRA PzF Stenting to Reduce Duration of Triple Therapy

COBRA-REDUCE
Start date: February 5, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether patients undergoing coronary intervention that also require oral anticoagulation, treatment with the COBRA PzF stent plus 14-day dual anti-platelet therapy (DAPT) has higher safety and non-inferior outcomes for thrombo-embolic events than compared with standard FDA-approved drug eluting stent (DES) plus 3 or 6-month DAPT.

NCT ID: NCT02593838 Terminated - Clinical trials for Coronary Artery Disease

Dynamic CT Myocardial Perfusion Imaging

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

This study aims at evaluating the feasibility of CT myocardial perfusion imaging in daily clinical practice and compare it to SPECT perfusion imaging in order to assess sensitivity and specifity of CT myocardial perfusion imaging compared to SPECT.

NCT ID: NCT02593058 Completed - Schizophrenia Clinical Trials

Positive Emotions Program for Schizophrenia (PEPS)

PEPS-RCT
Start date: February 1, 2016
Phase: N/A
Study type: Interventional

This study evaluates the addition of a 8 session psychological program, called Positive Emotions Program for Schizophrenia (PEPS) to improve motivation and pleasure in adults with schizophrenia. Half of the participants will receive their usual treatment and PEPS in combination, while the other half will receive usual treatment only.

NCT ID: NCT02592707 Terminated - Clinical trials for Neuroendocrine Tumors

Study to Evaluate the Safety and Preliminary Efficacy of 177Lu-OPS201 in NETs

Start date: March 6, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this clinical phase I/II study was to investigate the safety and tolerability of satoreotide tetraxetan (177Lu-IPN01072, formerly known as 177Lu-OPS201) used for the treatment of patients with neuroendocrine tumors (NETs). The secondary objectives of this study were the assessment of biodistribution, dosimetry and preliminary efficacy of satoreotide tetraxetan.

NCT ID: NCT02591927 Not yet recruiting - Clinical trials for Myocardial Infarction

Reappraisal of GIK in Acute STEMI by Pre-hospital Administration

REAGIK-STEMI
Start date: February 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is: 1. to assess whether pre-hospital glucose-insulin-potassium (GIK) administration in acute STEMI patients would reduce infarct size and ischemia/reperfusion damage using comprehensive tissue characterization by cardiovascular magnetic resonance (CMR) at an early post-infarction phase. 2. to explore the putative cardioprotective mechanisms of pre-hospital GIK administration

NCT ID: NCT02591043 Completed - Fracture Clinical Trials

Surgical Treatment of Low Energy Pelvic Fractures in the Elderly

PelvicRetro
Start date: October 2015
Phase: N/A
Study type: Interventional

Since May 2010 the Department of Trauma, Basel University Hospital has performed surgical stabilisation of the posterior pelvic ring on 55 patients. These patients have not received a structured follow up examination or evaluation of outcome after surgery.