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NCT ID: NCT02252107 Completed - Clinical trials for Acute Myeloid Leukemia (AML)

10-day Decitabine, Fludarabine and 2 Gray TBI as Conditioning Strategy for Poor and Very Poor Risk AML in CR1

Start date: October 2014
Phase: Phase 2
Study type: Interventional

This study examines whether the addition of decitabine to the standard Flu/TBI conditioning regimen prior to allogeneic stem cell transplantation in poor and very poor risk AML patients, reduces the risk of recurrence of the disease. Because decitabine has hardly any side effects, it will likely have little impact on the occurrence of Graft Versus Host Disease. The investigators are looking for a pre-treatment for transplantation which reduces the chance of recurrence of the disease without involving severe damage to normal tissues.

NCT ID: NCT02251964 Completed - Clinical trials for Lung Diseases, Interstitial

Rituximab in Interstitial Pneumonitis

RITUX-IP
Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This project will address rare immune mediated inflammatory diseases (IMIDs) involving the lungs, i.e. interstitial pneumonitis (IP). The main objective of this study is to assess the effects of rituximab (RTX) as a rescue therapy for progressive IMID-IP patients. The primary study parameter is pulmonary function. The secondary objectives are to explore the application of imaging with radiolabeled RTX as early predictor for efficacy of RTX, to study the effects of RTX treatment on quality of life, and to further elucidate the pathophysiology of IMID-IP by analyzing biochemical markers.

NCT ID: NCT02251275 Completed - Clinical trials for Polycystic Kidney, Autosomal Dominant

Long Term Safety of Immediate-release Tolvaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease

Start date: October 17, 2014
Phase: Phase 3
Study type: Interventional

The purpose of the trial was to evaluate and describe the long term safety of tolvaptan in participants with autosomal dominant polycystic kidney disease (ADPKD).

NCT ID: NCT02249975 Completed - Barrett's Esophagus Clinical Trials

Efficacy of CryoBalloon Focal Ablation System on Human Esophageal Barrett's Epithelium

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

The purpose of this study is to assess the efficacy and performance of the C2 Focal Cryoablation System in patients with BE.

NCT ID: NCT02249000 Completed - Clinical trials for Aortic Valve Stenosis

BIOVALVE - I / II Clincial Investigation

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

First-in-Human clinical investigation to evaluate the safety and clinical performance of the BIOVALVE prosthesis in subjects presenting with severe symptomatic aortic valve stenosis, which are as judged by the heart team, indicated for transfemoral transcatheter aortic valve implantation

NCT ID: NCT02248753 Completed - Atrial Fibrillation Clinical Trials

Acute Cardioversion Versus Wait And See-approach for Symptomatic Atrial Fibrillation in the Emergency Department

RACE 7 ACWAS
Start date: October 2014
Phase: N/A
Study type: Interventional

A symptomatic episode of the heart rhythm disorder 'atrial fibrillation' (AF) is a frequent reason for visits to the emergency department. Currently, in the majority of cases, immediate (electrical or pharmacological) cardioversion is chosen, while atrial fibrillation terminates spontaneously in 70% of the cases within 24 hours. A wait-and-see approach with rate-control medication only, and when needed cardioversion within 48 hours of onset of symptoms, could be effective, safe and more cost-effective than current standard of care and could lead to a higher quality of life.

NCT ID: NCT02248415 Completed - Coronary Disease Clinical Trials

Administration of Warm Blood Cardioplegia With or Without Roller Pump

Start date: September 2012
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of warm blood cardioplegia administration with and without roller pump on perioperative myocardial injury, reflected by postoperative biomarker release, in patients undergoing coronary artery bypass grafting (CABG) with a minimal extracorporeal circuit (MECC).

NCT ID: NCT02247349 Completed - Clinical trials for Small Cell Lung Cancer

BMS-986012 in Relapsed/Refractory SCLC

Start date: November 14, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, pharmacokinetics, immunogenicity, antitumor activity and pharmacodynamics of BMS-986012 alone and in combination with nivolumab in patients with relapsed/refractory SCLC.

NCT ID: NCT02247128 Completed - Stroke Clinical Trials

Antiplatelet Therapy for Patients Undergoing Transcatheter Aortic Valve Implantation

POPular-TAVI
Start date: January 2014
Phase: Phase 4
Study type: Interventional

At present, a variety of antithrombotic regimens are prescribed in the early postprocedure period after transcatheter aortic valve implantation (TAVI). Dual antiplatelet therapy (DAPT) using aspirin and a thienopyridine in the initial period after TAVI is the recommended strategy; however, mono antiplatelet therapy using aspirin is suggested not to be inferior. In patients with atrial fibrillation (AF) or another indication for oral anticoagulation (OAC), no recommendations on best treatment regimen currently exist although triple therapy (OAC + DAPT) is best avoided due to increased bleeding risk. We hypothesise that the omission of clopidogrel in the first 3 months after TAVI is safer and not less beneficial than the addition of clopidogrel to aspirin (cohort A) or OAC (cohort B).

NCT ID: NCT02246179 Completed - Clinical trials for Local Anesthesia of the Skin.

Fractional Laser Assisted Delivery of Anesthetics

Start date: September 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy of fractional CO2 laser assisted delivery of topically applied anesthetics (articaine hydrochloride 40 mg/ml and epinephrine 10 μg/ml solution and EMLA cream) regarding to anesthesia of the skin.