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NCT ID: NCT02041052 Terminated - Clinical trials for 50 % Reduction of Delayed Gastric Emptying

The Size of the Gastric Remnant as Determinant for Delayed Gastric Emptying After Whipple Resection.

Start date: January 2013
Phase: Phase 2
Study type: Interventional

A small gastric remnant after whipple resection improves gastric emptying and therefore prevents the development of delayed gastric emptying.

NCT ID: NCT02040909 Terminated - Clinical trials for Anesthesia Intubation Complication

Optimizing Propofol Dosing for (Preterm) Newborn Infants That Need Endotracheal Intubation

NEOPROP2
Start date: July 2014
Phase: Phase 1
Study type: Interventional

Newborns admitted to an intensive care unit often require artificial ventilation. For that purpose an endotracheal tube needs to be placed into the trachea, a procedure named endotracheal intubation. The newborns need to be sedated to keep them comfortable, to stop moving and to relax in order to enable the success of the procedure. For this sedation an anesthetic agent named propofol is often used. The used dose of propofol has not been properly studied and as a consequence patients are under- or over -sedated and propofol leads to side effects such as hypotension. The current study aims to find the most appropriate dose of propofol for newborns of different gestational ages and of different post-natal ages. We will use propofol in different doses and after each 5 included patients per age group we will analyze whether the dose needs to be increased or decreased. The effect of the propofol will be extensively monitored and we will study the level of sedation, the quality of intubation, the stability of the patient en the occurrence of side effects. At the end we aim to have appropriate guidelines for propofol doses in newborns of all ages.

NCT ID: NCT02039713 Terminated - Clinical trials for Coronary Artery Disease

DESyne in Routine Clinical Practice

IRIS DESYNE
Start date: July 2014
Phase:
Study type: Observational

The purpose of this study is to evaluate effectiveness and safety of DESyne in Routine Clinical Practice

NCT ID: NCT02039167 Terminated - Atrial Fibrillation Clinical Trials

Left Atrial Appendage Occlusion vs. Usual Care in Patients With Atrial Fibrillation and Severe Chronic Kidney Disease

WatchAFIB
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the superiority of left atrial appendage occlusion in comparison to oral anticoagulation with a vitamin K antagonist (INR 2-3) related to the frequency of occurrence of at least one bleeding classified as moderate or major within 24 months.

NCT ID: NCT02038153 Terminated - Clinical trials for Adult Acute Myeloid Leukemia in Remission

Lenalidomide in Treating Older Patients With Acute Myeloid Leukemia Who Have Undergone Stem Cell Transplant

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best dose of lenalidomide and how well it works in treating older patients with acute myeloid leukemia (AML) who have undergone stem cell transplant. Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing.

NCT ID: NCT02038049 Terminated - Clinical trials for Relapse Remitting Multiple Sclerosis

A Study to Assess the Effect of a Single Infusion of VAY736 on Disease Activity in Patients With Relapsing-remitting Multiple Sclerosis

Start date: December 20, 2013
Phase: Phase 2
Study type: Interventional

This was a randomized, partially blinded, placebo-controlled, non-confirmatory study to assess the effects of a single infusion of VAY736 on disease activity as measured by brain MRI scans in patients with relapsing-remitting multiple sclerosis (RRMS).

NCT ID: NCT02037412 Terminated - Clinical trials for Acute Coronary Syndrome

Impact of Ticagrelor on the Endothelial Healing Following Drug-eluting Stent Implantation in the Patients With Acute Coronary Syndrome

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

The investigators hypothesized that ticagrelor may enhance endothelial healing after DES implantation by increasing adenosine concentrations by the inhibition of adenosine uptake into erythrocytes, compared to clopidogrel. Thus, the investigators will evaluate the extent of endothelialization (stent strut coverage) and neointimal hyperplasia (neointimal thickness) 3 months after DES implantation by optical coherence tomography (OCT)

NCT ID: NCT02036697 Terminated - Clinical trials for Hemodynamic Instability

Hemodynamic Effects of Low Dose Spinal Anesthesia for Cesarean Section

Start date: November 2013
Phase: N/A
Study type: Interventional

We propose to study the effects on hemodynamics (blood pressure, cardiac output, and central venous pressure) of two doses of bupivacaine for spinal anesthesia during cesarean section: a higher dose of 12 mg to a lower dose of 4.5 mg. We will examine recovery times, incidence of hypotension, and compare pain control and maternal satisfaction during and after cesarean section. We hypothesize that low dose bupivacaine spinal anesthesia will provide equivalent anesthesia for cesarean section compared to conventional dose bupivacaine, with less hypotension, faster recovery time, and enhanced maternal satisfaction. Maternal satisfaction will be assessed by self-reported pain scores, incidence of nausea and vomiting, shivering, and ability to interact with baby in the OR.

NCT ID: NCT02035345 Terminated - Clinical trials for Recurrent Ovarian Cancer

Slowed Carboplatin Infusion for Ovarian Cancer Patients Receiving Carboplatin Re-Treatment

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

This is a research study to determine if administering carboplatin at a slower rate when re-treating recurrent ovarian cancer patients prior to the development of a hypersensitivity reaction will decrease the frequency and severity of future hypersensitivity reactions.

NCT ID: NCT02033278 Terminated - Clinical trials for Idiopathic Dilated Cardiomyopathy

Infusion Intracoronary of Mononuclear Autologous Adult no Expanded Stem Cells of Bone Marrow on Functional Recovery in Patients With Idiopathic Dilated Cardiomyopathy and Heart Failure.

Start date: January 6, 2014
Phase: Phase 2
Study type: Interventional

Clinical trial phase IIb, double-blind, randomized, controlled with placebo. There is sufficient preliminary evidence to consider intracoronary injection of bone marrow progenitor cells as a viable, safe and beneficial treatment in patients with dilated cardiomyopathy, although the biological mechanism of action of bone marrow cells in the myocardium is not known. In this project we propose to investigate comparatively and from a biological and clinical point of view the applicability of regenerative therapy with autologous bone marrow cells in patients with dilated cardiomyopathy.