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NCT ID: NCT03592940 Completed - Mediterranean Diet Clinical Trials

The Management of Neuroendocrine Tumours: A Nutritional Viewpoint.

NetNutr
Start date: November 1, 2017
Phase:
Study type: Observational

Nutritional status in patients with neuroendocrine tumours (NETs), especially of gastroenteropancreatic origin, can be deeply affected by excessive production of gastrointestinal hormones, peptides, and amines, which can lead to malabsorption, diarrhoea, steatorrhea, and altered gastrointestinal motility. Besides, the surgical and/or medical management of NETs can lead to alteration of gastrointestinal secretory, motor, and absorptive functions, with both dietary and nutritional consequences. Indeed, disease-related malnutrition is a frequently encountered yet both underrecognized and understudied clinical phenomenon in patients with NETs, with substantial prognostic and socioeconomic consequences. Most of these conditions can be alleviated by a tailored nutritional approach, also with the aim of improving the efficacy of cancer treatments. In this setting, skilled nutritionists can play a fundamental role in the multidisciplinary health care team in NETs management and their presence should be recommended.

NCT ID: NCT03592836 Completed - Clinical trials for Heart Failure NYHA Class III

Diuretic Response in Advanced Heart Failure: Bolus Intermittent vs Continuous INfusion

DRAIN
Start date: May 1, 2013
Phase: Phase 3
Study type: Interventional

Loop diuretics are the main therapy for decongestion of patients with advanced acute heart failure. However, these patients often develop diuretic-resistance or even diuretic-refractoriness. In order to overcome such resistance to diuretic, the clinician can increase the dose of furosemide, or change the way of administration (continuous infusion versus boluses) or associate a different class of diuretics (thiazide diuretics, K+-sparing diuretics) up to the addition of low doses of inotropic agents to improve renal perfusion. At the present time there is no evidence in literature in advanced acute heart failure patients about the superiority of the treatment with furosemide in continuous infusion or in intermittent boluses. The aim of the study was to evaluate the efficacy of furosemide in boluses versus continuous infusion in advanced acute heart failure.

NCT ID: NCT03592758 Completed - Clinical trials for Airway Complication of Anesthesia

Ultrasound in Evaluation of Difficult Airway Management Predictive Indexes

Start date: June 1, 2017
Phase:
Study type: Observational

evaluate the efficacy of the ultrasound approach in predicting difficult mask ventilation in a heterogeneous population of patients undergoing general anesthesia.

NCT ID: NCT03592420 Completed - Stroke Clinical Trials

PRE.C.I.S.A - Fall Prevention and Promotion of Active and Healthy Aging

PRECISA
Start date: December 31, 2014
Phase: N/A
Study type: Interventional

Randomized Controlled Trial (RCT) aiming at assessing the efficacy of an interdisciplinary multi-component and personalized multi-factorial intervention for reducing falls at one year post-enrolment in comparison to the usual care in a sample of community dwelling elderly (age ≥65 years), with or without Parkinson's Disease and/or previous Stroke.

NCT ID: NCT03591029 Completed - Heart Diseases Clinical Trials

Evaluation of PCO2 and PO2 Values in the Pulmonary Artery and Superior Vena Cava

Start date: July 19, 2018
Phase:
Study type: Observational

The study is about comparing blood samples obtained from the superior vena cava and the pulmonary artery. The investigators will compare the values of PCO2 and PO2 from these two sites, in order to see if exists a PCO2 gap and a PO2 gap, different from zero. Moreover the investigators want to find out if these gaps are related with changes in the cardiac output, the hematocrit or if they can predict post operative dysfunctions. Blood samples will be taken at six different times as scheduled by the protocol. Along with the two venous blood samples, an arterial blood sample will be taken too, from a radial of femoral artery catheter.

NCT ID: NCT03590314 Completed - Stroke Clinical Trials

Upper Limb Training Modalities in Patients With Stroke

Start date: January 2017
Phase: N/A
Study type: Interventional

To date, evidence of the effects of robotic training combined with OnabotulinumtoxinA focal treatment for spasticity is limited. The objective of this study were to compare the effects of robotic training against conventional rehabilitation on functional recovery, strength and spasticity, in stroke patients who underwent OnabotulinumtoxinA focal treatment for spasticity. We performed a single-blind, randomized, controlled trial involving 24 outpatients with diagnoses of stroke, divided in two groups (experimental and control group). Experimental group received specific robotic training for the upper limb with the device Armotion/Motore (Reha Technology AG, Olten, Switzerland). Our primary outcome was Fugl-Meyer Assessment Motor Scale (FMA). Secondary outcome were Action Research Arm Test (ARAT), Modified Ashworth Scale (MAS), Medical Research Council Scale (MRC) and surface Electromyography (EMG). 14 healthy age-matched controls underwent one session of sEMG acquisition to collect normative data.

NCT ID: NCT03590275 Completed - Clinical trials for Pancreatic Cancer Non-resectable

Observational Retrospective Study of Evaluation of Prognostic Factors in Advanced Pancreatic Cancer Patients Treated With FOLFIRINOX

HOPE
Start date: October 2, 2017
Phase:
Study type: Observational

The aim of this study is to identify new prognostic factors in patients affected by advanced pancreatic carcinoma treated with first line chemotherapy with FOLFIRINOX regimen. Primary objective is the identification of clinical, laboratory and pathologic factors affecting overall survival of these patients.

NCT ID: NCT03590093 Completed - Clinical trials for Periodontal Diseases

Amelogenins and Systemic Inflammation After Periodontal Surgical Therapy

PERIOEMD-1
Start date: November 1, 2013
Phase: N/A
Study type: Interventional

The aim of this study is to compare surgical treatment of periodontal infrabony defects with and without the adjunct of an enemal matrix derivative (EMD) in terms of acute-phase responses, in systemic healthy patients.

NCT ID: NCT03589469 Completed - Clinical trials for Diffuse Large B-cell Lymphoma Recurrent

Study to Evaluate the Efficacy and Safety of Loncastuximab Tesirine in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

LOTIS-2
Start date: August 1, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this Phase 2 study is to evaluate the clinical efficacy and safety of Loncastuximab Tesirine (ADCT-402) in patients with relapsed or refractory Diffuse Large B-Cell Lymphoma.

NCT ID: NCT03589391 Completed - Clinical trials for Non Invasive Monitoring of Loss of Resistance During Epidural Injection

New Mechatronic Device for Epidural Space Detection

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

This study sought to perform the feasibility assessment of a new, non-invasive device for Loss of Resistance (LOR) detection in clinical settings. The device in charge is a mechatronic device optimized in its configurations in order to detect Loss of Resistance while performing epidural injections.