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NCT ID: NCT03351712 Recruiting - Health Behavior Clinical Trials

mACTonHEALTH: Psychological Flexibility and Activity Tracker - Protocol

ACTonHEALTH
Start date: November 11, 2020
Phase: N/A
Study type: Interventional

Obesity and overweight are growing steadily and becoming a global epidemic. Recent researches report a 64% of the adult population as overweight. The social and economical impact is increasing and the most of the rehabilitation programs, while effective in the short term, do not produce long lasting results. From a behavioral perspective an explanatory model can describe the phenomena with the lack of sources of reinforcement related to healthy habits in the daily-life context. The goal of this project, combining Acceptance and Commitment Therapy and Wearable Technology, is to develop an effective intervention, efficient and sustainable, which continues after ending of the hospitalization, providing adequate contingencies of reinforcement in the natural environment, integrating systematic measurements, continuous feedbacks and individualized, values-based objectives. Related goal-setting show a shift from results linked with weight loss towards action connected with healthy life-style.

NCT ID: NCT03350412 Recruiting - Clinical trials for Metastatic Colorectal Cancer

Genotyping of Metastatic Colorectal Cancer Patients for Precision Medicine Clinical Trials

FUNNEL
Start date: October 2015
Phase:
Study type: Observational

The goal of delivering the right drug to the right cancer patient (precision medicine) requires a detailed understanding of how genomic alterations are linked to drug response. The purpose of this study is to intercept at point-of-care a large cohort of newly diagnosed mCRC patients to determine if it is possible to obtain personalized genetic information from each subject's tumor (tissue and blood) to triage treatment choices. In case of target positivity, patients will be conveyed, whenever possible, to self-standing, independent, hypothesis-driven POC trials as soon as they exhibit resistance to standard of care treatment.

NCT ID: NCT03347318 Recruiting - Solid Tumors Clinical Trials

Target Therapies Resistance Molecular Profiling in Patients With Neoplastic Disease

PROFILING
Start date: January 2011
Phase: N/A
Study type: Observational

The main purpose of this study is to define the molecular profile of selected solid tumors. From each participants will be collected biological materials for molecular analysis, including saliva, blood and vital tumor tissue derived form surgical or biopsy procedures. Whereas possible, vital tumor specimens will be inoculated and propagated in immunocompromised NOD/SCID mice to study the genetic correlations between genetic status and response to target drugs.

NCT ID: NCT03346018 Recruiting - Uveitis Tuberculous Clinical Trials

Immunologic Markers for the Differential Diagnosis Between Uveitis-TBC and Uveitis-SARC (TBC-SARC)

TBC-SARC
Start date: November 3, 2017
Phase:
Study type: Observational

Today there are no tests that allow to make a precise differential diagnosis between uveitis from presumed tuberculous origin and uveitis by sarcoidosis. Therefore, with this study, investigators aim to identify, in the aqueous humor and in the blood of participants (patients that suffering from one of these two forms of uveitis) the presence of immunologic markers that distinguish between uveitis of tuberculous etiology and uveitis by sarcoidosis.

NCT ID: NCT03344731 Recruiting - Brain Damage Clinical Trials

Cognitive Abilities in Brain Damaged Patients

Cog
Start date: December 15, 2017
Phase: N/A
Study type: Interventional

The presence of damage to the central and / or peripheral nervous system resulting from pathologies of a different nature (such as multiple sclerosis, Parkinson's disease, dementia, cranial trauma, stroke, epilepsy or other neurological syndromes) is commonly a cause of physical and mental disability. The presence of memory or language cognitive deficits is often evident at a first clinical examination. However, difficulties in cognitive areas such as decision-making, social and emotional cognition or particular forms of learning may be less evident, while exerting a strong impact on the quality of life of patients. The main purpose of this proposal is to investigate cognitive abilities in patients with neurological damage, through a series of specific tasks. In addition, the contribution of specific brain areas to the cognitive tasks will be assessed by direct modulation of brain activity. This modulation will be achieved by using non-invasive brain stimulation techniques such as Transcranial Magnetic Stimulation (TMS) and Direct Transcranial Electric Stimulation (tDCS).

NCT ID: NCT03343899 Recruiting - Clinical trials for Intervertebral Disk Degeneration

Genotype-related Molecular Targets in the Vitamin D Pathway for Spinal Disc Diseases

GenVDisc
Start date: February 17, 2016
Phase: N/A
Study type: Observational

The objective of our study will be to analyze the interplay between particular VDR variants and its ligand in cells obtained from intervertebral disc and cartilage endplate and their action on cell proliferation and phenotype maintenance. The identification of novel molecular targets in the vitamin D pathway, potentially promoting pathological alterations of the tissues involved in spinal disc diseases, will allow to develop innovative and more personalized preventive and pharmacological/nutritional therapies.

NCT ID: NCT03343470 Recruiting - Cushing Syndrome Clinical Trials

The Circadian Rhythm in CusHing SyndrOme in Active Phase and dUring RemiSsion (TheHOURS)

TheHOURS
Start date: November 8, 2017
Phase:
Study type: Observational

This is an observational, open, prospective multi-centre study designed to evaluate melatonin and cortisol circadian rhythm, immunological profile and anthropometric parameters in Cushing Syndrome patients during active Remission state.

NCT ID: NCT03340688 Recruiting - Preterm Birth Clinical Trials

Cerclage for Twins With Short Cervical Length ≤ 15mm

TWIN-UIC
Start date: June 22, 2017
Phase: N/A
Study type: Interventional

This is a multicenter randomized study designed to determine if ultrasound indicated cerclage reduces the incidence of spontaneous preterm birth <34 weeks in asymptomatic women with twin gestations and cervical length ≤15mm, diagnosed by transvaginal ultrasound between 16 to 23 6/7 weeks of gestation.

NCT ID: NCT03339115 Recruiting - Clinical trials for Mitral Regurgitation

AHEAD: European Feasibility Study of the Cardiovalve Transfemoral Mitral Valve System

AHEAD
Start date: April 23, 2018
Phase: N/A
Study type: Interventional

This study will evaluate the safety of the Cardiovalve Transfemoral Mitral Valve System with its associated procedure, and observe the device performance in reducing mitral regurgitation. Data collected in this clinical study will include 30-day safety and performance, and long-term clinical outcomes over a follow-up of 2 years.

NCT ID: NCT03339063 Recruiting - Clinical trials for Nontuberculous Mycobacteria

The Italian REgistry of Pulmonary Non-tuberculous mycobactEria

IRENE
Start date: April 21, 2017
Phase:
Study type: Observational [Patient Registry]

The Italian registry of pulmonary non-tuberculous mycobacteria (NTM) -IRENE- is an observational, multicenter, prospective, cohort study enrolling consecutive adult patients with either a NTM respiratory infection or NTM-Pulmonary Disease. The coordinating center is located at the Pulmonary Department of the Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy. So far, more than 35 centers, including mainly pulmonary and infectious disease departments, joined the registry. The registry has been developed to accept an unlimited number of patients and no deadlines have been decided.