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NCT ID: NCT02470143 Completed - Clinical trials for Coronary Artery Disease

a Bike Application to Support Cardiac Patient

BackonBike
Start date: August 2015
Phase:
Study type: Observational

The pilot study will investigate the usability of a mobile cycling application in a cardiac patient population during a one month study period. The application's effectiveness regarding ability to reduce fear and increase motivation to exercise will be assessed.

NCT ID: NCT02469623 Completed - Clinical trials for Supraventricular Tachycardia

Dipole Density Mapping in Supraventricular Tachycardia

DDRAMATIC-SVT
Start date: September 6, 2014
Phase: N/A
Study type: Interventional

Use of dipole density mapping to identify activation in complex supraventricular tachycardias.

NCT ID: NCT02469246 Completed - HIV-1 Infection Clinical Trials

Switch Study to Evaluate F/TAF in HIV-1 Infected Adults Who Are Virologically Suppressed on Regimens Containing ABC/3TC

Start date: June 29, 2015
Phase: Phase 3
Study type: Interventional

The primary objectives of this study are to evaluate the efficacy, safety, and tolerability of switching abacavir/lamivudine (ABC/3TC) fixed-dose combination (FDC) tablets to emtricitabine/tenofovir alafenamide (F/TAF) FDC tablets versus maintaining ABC/3TC in human immunodeficiency virus type 1 (HIV-1) infected adults who are virologically suppressed on regimens containing ABC/3TC.

NCT ID: NCT02468674 Completed - Sarcopenia Clinical Trials

A 24-week Off-drug Extension Study in Sarcopenic Elderly Who Completed Treatment in the 6-month Core Study

Start date: July 22, 2015
Phase: Phase 2
Study type: Interventional

This extension study was a 24-week off-drug follow-up of the core CBYM338E2202 (NCT ) study and the main objective was to determine the long-term durability of bimagrumab (BYM338) effect after a 6-month treatment period.

NCT ID: NCT02468115 Completed - Influenza Clinical Trials

Influenza Challenge Study of VIS410 in Healthy Volunteers

Start date: May 2015
Phase: Phase 2
Study type: Interventional

A phase 2 a study to assess the safety profile and the effect of VIS410 in healthy subjects after inoculation with influenza A virus (H1N1).

NCT ID: NCT02468076 Completed - Cholangiocarcinoma Clinical Trials

Radiofrequency Ablation for Biliopancreatic Malignancy

IGNITE-1
Start date: November 2014
Phase: Phase 2
Study type: Interventional

This phase-2 study aims to evaluate feasibility, safety and efficacy of thermal ablation of biliary obstructive malignancies by means of radiofrequency ablation (RFA, ELRA, StarMed) during endoscopic retrograde cholangio-pancreaticography (ERCP) with primary intent to obtain palliative biliary drainage via stenting

NCT ID: NCT02467062 Completed - Clinical trials for Aortic Valve Disease

Implementation of Non-size Markers Derived From 4D Flow MRI of Patients With Aortic Disease.

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

The aim of the investigator is to implement 4D FLOW MRI technique into a clinical setting and evaluate the blood flow pattern and wall sheer stress in patients with aortic and/or aortic valve diseases.

NCT ID: NCT02467049 Completed - Cancer Clinical Trials

ECG Versus Ultrasound-guided Positioning of the Peripherally Inserted Central Catheter (PICC) Tip

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

In the prevention of thrombosis related to catheter placement it is important to have a right position of the catheter tip. Therefor we want to assess which technique is the most successful in the placing of a PICC.

NCT ID: NCT02466815 Completed - Healthy Clinical Trials

A Study to Assess the Relative Bioavailability of JNJ-42756493 Tablets

Start date: June 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the relative bioavailability of 2 prototype G-025 tablets compared with the current G-018 tablet.

NCT ID: NCT02466321 Completed - Clinical trials for Cuff-tear Arthropathy

Anatomical Shoulderâ„¢ Inverse/Reverse Study

Start date: September 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to obtain outcomes data on the Anatomical Shoulderâ„¢ Inverse/Reverse System by analysis of standard scoring systems and radiographs. Outcome data will be collected using the following standard scoring systems of which summary statistics will be provided: - Constant and Murley Score to evaluate clinical parameters such as range of motion, power, level of pain and functional ability. - SF-12 Physical and Mental Health Summary Measures (SF12 Questionnaire) comprising of twelve questions to assess the subject's physical and mental health status which must be answered by the patient.