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NCT ID: NCT02228122 Completed - Diabetes Clinical Trials

The Effect of Aquacel® Ag+ Extra Dressing on Wound Biofilms

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

The purpose of the research is to assess the effects of Aquacel Ag+ Extra dressing on chronic wound bacterial biofilms

NCT ID: NCT02227992 Completed - Hemorrhage Clinical Trials

The EVARREST® Paediatric Mild/Moderate Liver and Soft Tissue Bleeding Study

Start date: July 1, 2014
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the safety and effectiveness of EVARRESTâ„¢ Sealant Matrix (EVARRESTâ„¢ Fibrin Sealant Patch) (EVARRESTâ„¢) in controlling mild or moderate soft tissue & parenchymal bleeding during open hepatic, abdominal, pelvic, retroperitoneal, and thoracic (non-cardiac) surgery in paediatric patients.

NCT ID: NCT02227862 Completed - Type 1 Diabetes Clinical Trials

Non-inferiority Study to Compare the Efficacy and Safety of Mylan's Insulin Glargine With Lantus® in Type 1 Diabetes Mellitus Patients (INSTRIDE 1)

INSTRIDE 1
Start date: June 2014
Phase: Phase 3
Study type: Interventional

To test whether Mylan's insulin glargine once daily is non-inferior to Lantus® once daily (based on change in HbA1c from baseline to 24 weeks) when administered in combination with mealtime insulin lispro.

NCT ID: NCT02227758 Completed - Clinical trials for Intractable Chronic Migraine

Peripheral Nerve Stimulation Registry for Intractable Migraine Headache

Relief
Start date: September 2012
Phase:
Study type: Observational

The purpose of this study is to evaluate the long-term safety and performance of neurostimulation for the treatment of intractable chronic migraine as well as to detect infrequent complications or problems only apparent in "real-world" practice

NCT ID: NCT02227732 Completed - Clinical trials for Malignant Pleural Effusions

A Pilot Study Evaluating the Safety and Effectiveness of a New Pleural Catheter for the Medical Management of Symptomatic, Recurrent, Malignant Pleural Effusions

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

The purpose of this study is to determine whether a new catheter is safe and effective in treating malignant pleural effusions.

NCT ID: NCT02227706 Completed - Hemorrhage Clinical Trials

The Paediatric EVICEL® Soft Tissue and Parenchymal Organ Bleeding Study

Start date: August 1, 2014
Phase: Phase 3
Study type: Interventional

To evaluate the safety and effectiveness of EVICEL® Fibrin Sealant (Human) as an adjunct to achieve haemostasis during surgery in paediatric patients.

NCT ID: NCT02227550 Completed - Atrial Fibrillation Clinical Trials

Apixaban During Atrial Fibrillation Catheter Ablation: Comparison to Vitamin K Antagonist Therapy

AXAFA
Start date: December 2014
Phase: Phase 4
Study type: Interventional

Study objective is to demonstrate that anticoagulation with the direct factor Xa inhibitor apixaban is not less safe than Vitamin-K-antagonists (VKA) therapy in patients undergoing catheter ablation of non-valvular AF in the prevention of peri-procedural complications. The AXAFA trial will compare peri-ablational treatment with apixaban to peri-ablational treatment wit VKA in a randomized trial of patients undergoing catheter ablation of atrial fibrillation (AF).

NCT ID: NCT02227498 Completed - Clinical trials for Age Related Macular Degeneration

Argus II Retinal Prosthesis System Dry AMD Feasibility Study Protocol

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

The purpose of this study is to test the Argus II Retinal Prosthesis System in patients with severe age-related macular degeneration (AMD). The Argus II System has already been studied in completely blind patients with retinitis pigmentosa (RP). In RP patients, some cells of the retina are irrevocably damaged and the Argus II System has been found to restore some basic visual function. On these grounds, the device has received authorization for use on the European market (the CE certification) in 2011.

NCT ID: NCT02227381 Completed - Clinical trials for Learning Disabilities

Action Medical Research

Start date: February 2011
Phase:
Study type: Observational

Learning disability affects 3% of the population. Severe types of learning disability are more likely to have an underlying genetic cause but diagnosis is difficult because many different genetic abnormalities may be involved. Obtaining a diagnosis is important so that patients can be managed appropriately and their families can be given accurate information. We aim to use new types of genetic testing which will make it possible to screen for several different genetic abnormalities which cause learning disability at the same time, so improving the accuracy and speed of diagnosis in the group of patients with severe learning disability. We will focus particularly on patients where seizures and behavioural problems are also present.This will enable more patients to be diagnosed accurately, reduce the number of hospital appointments needed and ultimately be more cost- effective.

NCT ID: NCT02227355 Completed - Clinical trials for Idiopathic Parkinson's Disease

Evaluating the Effectiveness of Neupro® (Rotigotine) and L-dopa Combination Therapy in Patients With Parkinson's Disease

NEUPART
Start date: September 2014
Phase: N/A
Study type: Observational

This study aims to evaluate the effectiveness of Rotigotine and Levodopa combination therapy for younger and older patients with Parkinson's Disease under real life conditions. Effects on ability to perform activities of daily living, sleep, medication dose and other factors will be assessed.