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NCT ID: NCT02946827 Recruiting - Celiac Disease Clinical Trials

A Low FODMAPs Diet in Celiac Patients With Persistent Gastrointestinal Symptoms

Start date: January 2016
Phase: N/A
Study type: Interventional

FODMAPS (fructose, oligosaccharides, monosaccharides, disaccharides and polyols) are characterised as fermentable but poorly absorbed carbohydrates which enter the colon and are utilised by colonic bacteria. During fasting colonic nutrients are scarce but ingesting FODMAPS causes a rapid increase in carbohydrate which can overwhelm the microbiota's ability to utilise substrate. The excess reducing equivalents will generate hydrogen or methane. The principal symptoms are diarrhoea and abdominal distension. Patients with irritable bowel syndrome appear to benefit by restricting intake, possibly because they are hypersensitive to intestinal distension. The focus of the study is to evaluate if in celiac patients with persistent abdominal symptoms and with a correct gluten free diet, a low FODMAPs diet can improve their symptoms. Moreover the study would like to observe if a dietary restriction in FODMAPs carries the risk of nutritional inadequacy.

NCT ID: NCT02945917 Recruiting - ARDS Clinical Trials

Positive End-expiratory Pressure and Esophageal Catheter Optimal Calibration Volume in ARDS Patients

Start date: April 2015
Phase: N/A
Study type: Observational

The use of esophageal balloon catheter to estimate pleural pressure has gained renewed popularity in recent years. Indeed, measurement of transpulmonary pressure may allow a more pathophysiological-based approach to ventilator strategy in acute respiratory distress syndrome (ARDS) patients. Nevertheless, it is well known that esophageal balloon catheter derived parameters can be influenced by several patient-related or technical-related factors. During a PEEP trial, the investigators will observe in-vivo the esophageal pressure and derived measurements obtained using different esophageal balloon calibration volumes.

NCT ID: NCT02940600 Recruiting - Clinical trials for Ischemic Reperfusion Injury

Efficacy Evaluation of Normothermic Perfusion Machine Preservation in Liver Transplant Using Very Old Donors

CEFEMA
Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of normothermic machine perfusion in liver transplantation using grafts of brain death donors older or equal than 70 years

NCT ID: NCT02940054 Recruiting - Crohn's Disease Clinical Trials

RED-FLAGS Index Validation in Crohn's Disease Patients

RED-FLAGS2
Start date: February 2015
Phase: N/A
Study type: Observational

Observational prospective study to validate a new index for early diagnosis of Crohn's disease (CD)

NCT ID: NCT02938299 Recruiting - Malignant Melanoma Clinical Trials

Neoadjuvant L19IL2/L19TNF- Pivotal Study

Pivotal
Start date: July 1, 2016
Phase: Phase 3
Study type: Interventional

Phase III, open-label, randomized, controlled multi-center study of the efficacy of L19IL2/L19TNF neoadjuvant intratumoral treatment in Stage III B/C melanoma patients.

NCT ID: NCT02934464 Recruiting - Stomach Neoplasms Clinical Trials

Assessment of Ramucirumab Plus Paclitaxel as Switch MANteInance Versus Continuation of First-line Chemotherapy in Patients With Advanced HER-2 Negative Gastric or Gastroesophageal Junction Cancers

ARMANI
Start date: December 2016
Phase: Phase 3
Study type: Interventional

This is a randomized, open-label, multicenter phase III trial of ramucirumab plus paclitaxel, given as switch maintenance, versus continuation of first-line chemotherapy, given as per standard clinical practice, in subjects with unresectable locally advanced or metastatic HER-2 negative gastric or GEJ cancer, without disease progression following 3 months of first-line doublet chemotherapy. The acceptable first-line or lead-in chemotherapy will be: - FOLFOX4:Oxaliplatin 85 mg/m2. l-Leucovorin 100 mg/m2 5-fluorouracil 400/600 mg/m2. Cycle length is 2 weeks +/- 3 days. - ModifiedFOLFOX6: Oxaliplatin a 85 mg/m2. l-Leucovorin 200 mg/m2. 5-fluorouracil 400 mg/m2 and 2400 mg/m2 46-hours continous infusion. Cycle length is 2 weeks +/- 3 days. - XELOX:Oxaliplatin130 mg/m2.Capecitabine will be 2000 mg/m2 for 14 days. Cycle length is 3 weeks +/- 3 days.

NCT ID: NCT02932618 Recruiting - Clinical trials for Von Willebrand Disease

A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

Start date: December 18, 2017
Phase: Phase 3
Study type: Interventional

The main aim of the study is to check effectiveness, side effects, and tolerability of recombinant von Willebrand Factor (rVWF), with or without ADVATE, in the treatment and control of nonsurgical bleeding events in pediatric participants (less than (<)18 years of age) with severe hereditary von Willebrand disease (VWD). The participants will be treated with rVWF for 12-18 months. Their von Willebrand Disease will be treated by their doctor according to their doctor's usual clinical practice. During the study, participants will be followed up at clinics or over telephone calls.

NCT ID: NCT02932150 Recruiting - Chronic Hepatitis B Clinical Trials

Study of Tenofovir Alafenamide (TAF) in Children and Teen Participants With Chronic Hepatitis B Virus Infection

Start date: November 2016
Phase: Phase 2
Study type: Interventional

The goals of this clinical study are to compare the effectiveness, safety and tolerability of study drug, tenofovir alafenamide (TAF), versus placebo in teens and children with CHB and to learn more about the dosing levels in children.

NCT ID: NCT02931123 Recruiting - Clinical trials for Cirrhotic Patients Undergoing TIPS Placement

A RCT COMPARING LACTULOSE AND RIFAXIMIN ASSOCIATED WITH A VEGETABLE DIET IN THE PREVENTION OF POST-TIPS OVERT HEPATIC ENCEPHALOPATHY

Start date: November 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This is a randomized controlled trial whose purpose is to evaluate the efficacy of therapy with lactulose and rifaximin associated with a vegetable diet in the prevention of post-TIPS hepatic encephalopathy.

NCT ID: NCT02927756 Recruiting - Clinical trials for Non-Hodgkin Lymphoma Transformed Recurrent

Italian Multicenter Retrospective Observational Study on Transformed Lymphomas

FLT-Oss-2015
Start date: November 2017
Phase: N/A
Study type: Observational

Study purpose is to evaluate treatment outcome and survival in patient with aggressive lymphomas transformed from Follicular Lymphoma.