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NCT ID: NCT02712749 Completed - Anxiety Clinical Trials

Use of Binaural Beat Premedication in Elderly Submitted to Major Orthopedic Surgery

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The Investigators verify the effectiveness of "Binaural Beats" as premedication instrument in elderly patients submitted to orthopedic surgery to reduce anxiety , post operative pain and morphine consumption

NCT ID: NCT02711852 Completed - Clinical trials for Hematologic Malignancy

A Long-term, Continued Treatment and Follow-up Study in Participants With Hematologic Malignancies Treated With Duvelisib (IPI-145)

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

This was a long-term, continued treatment study that evaluated the long-term safety, clinical activity, and overall survival (OS) of duvelisib in individuals with hematologic malignancies that were previously treated with duvelisib in a previous sponsor-approved study.

NCT ID: NCT02711163 Completed - Cow Milk Allergy Clinical Trials

Evaluation of the Hypoallergenicity of an Extensively Hydrolyzed Formula

ALYCE
Start date: April 2016
Phase: Phase 3
Study type: Interventional

The aim of this study is to assess the hypoallergenicity of a new thickened extensively hydrolyzed formula, in infants with confirmed cow's milk protein allergy assessed through a double blind placebo controlled food challenge, followed by a 3-month open feeding period.

NCT ID: NCT02710890 Completed - Epilepsy Clinical Trials

Study to Investigate Safety and Tolerability of Intravenous Lacosamide in Children.

ASPIRE
Start date: May 30, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

EP0060 is a multicenter, open-label study to evaluate the safety and tolerability of intravenous (iv) Lacosamide (LCM) in pediatric subjects >= 1 month to < 17 years of age with epilepsy.

NCT ID: NCT02710643 Completed - Clinical trials for Follicular Lymphoma, Grade 1

"MIRO" Molecularly Oriented Immuno-radio-therapy

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

Phase II prospective multicenter study for stage I/II Follicular Lymphoma treated with involved-field radiotherapy (IFRT) at doses of 24 Gy) with or without Ofatumumab for 8 weekly doses on molecular basis. Patients with positive basal Bcl-2 will be followed every 3 months and with Bcl-2 detection every 6 months for 3 years. Patient with negative basal Bcl-2 will be followed every 3 months without further Bcl-2 detection. Ofatumumab treatment will be administered to: 1. Patients with positive basal PCR for Bcl-2-IgH rearrangement in BM and/or PB, resulting still positive after IFRT; 2. Patients with positive basal PCR for Bcl-2-IgH in

NCT ID: NCT02710591 Completed - Clinical trials for Muscular Dystrophy, Duchenne

Rimeporide in Patients With Duchenne Muscular Dystrophy

RIM4DMD
Start date: March 2016
Phase: Phase 1
Study type: Interventional

In Duchenne Muscular Dystrophy (DMD) there is an imbalance between the levels of calcium and sodium in the muscles cells which is thought to be important in the damage which occurs overtime. Sodium/proton type 1 exchanger (NHE-1) inhibition is an innovative pathway that has proved to efficiently prevent the accumulation of muscle damage (inflammation and fibrosis) in animal models of muscular dystrophies and heart failure. Based on prior safety and efficacy results in animal and humans, NHE-1 inhibition with Rimeporide represents a new therapeutic approach with no restriction on age and on genetic subtypes which could be combined to other treatments that restore or augment dystrophin.This study examines the safety and tolerability and effects on the muscles of rimeporide, in patients aged 6 to 14 years with Duchenne Muscular Dystrophy (DMD).

NCT ID: NCT02710513 Completed - Healthy Clinical Trials

ProAliFun_6.5_Health Effects of a Functional Pasta Enriched With Barley Beta-glucans on Healthy Subjects

ProAliFun65
Start date: December 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the healthy properties of a dietary intervention based on an innovative pasta enriched with prebiotic fibers (barley beta-glucans). The hypothesis is that the gut microbiota and metabolome, the nutritional status, the redox/subclinical inflammation parameters and the markers of cardiovascular risk may improve in healthy subjects.

NCT ID: NCT02709824 Completed - Adverse Effect Clinical Trials

Anti-staining Efficacy of Anti-Discoloration System (ADS) Added to Chlorhexidine (CHX)

CHX+ADS
Start date: December 2011
Phase: N/A
Study type: Interventional

Dental staining is the most common local side effect of chlorhexidine (CHX) mouthwashes. A prospective, cross-over, randomized clinical trial will be carried out in triple blind to compare the effect on dental staining of two 0.12% CHX mouthwashes: with or without ADS. Twenty-two healthy subjects will be enrolled. Briefly, the study includes two sequential stages: in the first phase, we record the "immediate" objective and subjective evaluation of dental discoloration by spectroscopic and questionnaire-based analyses, at baselines and after each 21 days long-cycle of mouthwash. A wash-out period between the cycles of 21 days is performed. In the second phase, a long-term (after 6 months) subjective evaluation of dental discoloration was obtained by means of clinical photograph visual analysis and new questionnaires.

NCT ID: NCT02709746 Completed - Clinical trials for Depressive Disorder, Major

Active Reference (Fluoxetine) Fixed-dose Study of Vortioxetine in Paediatric Patients Aged 12 to 17 Years With Major Depressive Disorder (MDD)

Start date: May 2016
Phase: Phase 3
Study type: Interventional

Evaluating the efficacy of vortioxetine 10 mg/day and 20 mg/day versus placebo on depressive symptoms in adolescents (age ≥12 and ≤17 years) with a DSM-5™ (Diagnostic and Statistical Manual of Mental Disorders, 5th edition) diagnosis of Major depressive disorder (MDD).

NCT ID: NCT02709681 Completed - Sickle Cell Disease Clinical Trials

Hydroxyurea in the Treatment of Sickle Cell Disease

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

This is a retrospective cohort study of Sickle Cell Disease (SCD) patients attending 32 treatment centers across Italy. The aim of this study will be to report the Italian experience with the use of hydroxyurea in a large cohort of SCD patients and to evaluate the benefits and safety of this intervention for the prevention and management of a wide range of clinical morbidities