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NCT ID: NCT03070457 Not yet recruiting - Morbid Obesity Clinical Trials

Safety of an Early Discharge Protocol After Sleeve Gastrectomy

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

Evaluate the safety and efficacy of an early discharge protocol (23 hours, overnight stay) after scheduled sleeve gastrectomy.

NCT ID: NCT03045042 Not yet recruiting - Pompe Disease Clinical Trials

Search for Serum/Plasma Biomarkers in Pompe's Disease

BIOPOMPE
Start date: April 2017
Phase: N/A
Study type: Observational

This study aims to analyze serum and plasma samples from patients with late onset Pompe disease treated and not treated with enzyme replacement therapy (ERT) to identify microRNA that could be specific of the disease. The investigators will correlate the concentration of these microRNA with several muscle function tests and quantitative muscle MRI to know whether they are good biomarkers of progression.

NCT ID: NCT02991287 Not yet recruiting - Clinical trials for Chronic Postoperative Pain

Validation of Predictive Scale of Chronic Postsurgical Pain

Start date: February 2017
Phase: N/A
Study type: Observational

To asses the precision of a score to predict chronic post surgical pain in patients undergoing inguinal hernia repair, abdominal hysterectomy, vaginal hysterectomy and thoracotomy. Prospective multicenter cohort study in 21 hospital in spain.

NCT ID: NCT02889406 Not yet recruiting - Childhood Obesity Clinical Trials

Motivation Approach for Childhood Obesity Treatment

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

In a recent study, we have demonstrated that the motivational therapy approach to treat childhood obesity is highly effective at clinical and metabolic levels. This efficacy has been proved in a clinical outpatient setting. However, a standardized collaborative approach between the clinic and the primary care services would allow a faster and easier approach to childhood obesity treatment. Furthermore, this motivational and educational intervention would benefit from the current technologic facilities, the long term effect of the education at group level, in terms of food shopping plan, healthy, fast and cheap cooking methods that would be useful specially in low income families (with a higher prevalence of childhood obesity). The aim of this study is assessing the clinical and metabolic efficacy of a family intervention, coordinated between the clinical and primary care services from the Tarragona health-care region, using a motivational therapy at individual and group levels, which involves e-Health tools (wearable), focusing on families with an 8 to 13 years old obese child. The design will be a clustered randomized control trial, with an intervention group that will receive a multicomponent motivational and educational plan which will be compared to a control group receiving the usual recommendations performed in primary care centres (n=167 per group). The treatment of both study groups will last 12 months and will be performed at the primary care centres. In parallel, the study team will validate the methodology used to assess body composition in obese children as well as the changes produced by the intervention.

NCT ID: NCT02745132 Not yet recruiting - Hepatitis C Clinical Trials

Cognitive Impairments in Chronic Hepatitis C Patients and Potential Reversibility With New Agents (CICHepC)

CICHepC
Start date: June 2016
Phase: Phase 4
Study type: Interventional

The overall aim of this study is to evaluate the prevalence of cognitive impairments and brain anomalies in Chronic Hepatitis C infected individuals and to investigate likely changes in cognition and brain structure and function after treatment with Direct-acting Antivirals (DAAs).

NCT ID: NCT02732002 Not yet recruiting - Clinical trials for Shoulder Impingement

Functional and Clinical Screening Assesment of the Shoulder Complex A New Methodological Model for Injury Management

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

Work-related injuries of the shoulder complex represent a challenge for clinicians due to the large variety of clinical entities involved and the broad anatomic structures that are potentially affected. Furthermore, commonly performed orthopedic tests have demonstrated limited accuracy for the actual diagnosis of the injury. Although considerable research has been performed to standardize a model for shoulder injury management, a comprehensive approach integrating both a clinical and functional based status of the pathology and adapted rehabilitation prescription remains lacking. The present study protocol aims to complement previously published shoulder injury management algorithms. Potentially, the multi-component, individualized and progressive multi-etiologic shoulder injury management model for rehabilitation could become a new effective strategy for reducing the time required to regain functional capacity and symptom recovery among patients with work-related shoulder injuries.

NCT ID: NCT02718989 Not yet recruiting - Spasticity Clinical Trials

Modulation of H-reflex After Application of Electric Currents in Healthy People

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

The purpose of this study is to determinate whether the application of electric currents produce changes in the excitability of alpha moto neurone. Moreover evidence whether the effect of the electric currents can change the tone of the muscle under stimulation in healthy volunteers

NCT ID: NCT02707120 Not yet recruiting - Clinical trials for Neurotrophic Keratitis

Efficacy and Safety of Plasma Rich in Growth Factors (PRGF-Endoret) Eye-drops in the Treatment of Neurotrophic Keratitis

Start date: January 4, 2018
Phase: Phase 4
Study type: Interventional

Neurotrophic keratitis (NK) is a rare degenerative corneal disease caused by altered innervation of the trigeminal nerve that leads to rupture of the corneal epithelium, the regeneration deterioration and development of corneal ulceration, their fusion, and perforation The main characteristic in the NK is a decrease or absence of corneal sensitivity.

NCT ID: NCT02698618 Not yet recruiting - Clinical trials for Diabetes Mellitus, Type 2

PRotective Effect on the Coronary Microcirculation of Patients With DIabetes by Clopidogrel or Ticagrelor

PREDICT
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Ticagrelor has a protective effect on microcirculation during percutaneous coronary interventions in patients with Diabetes mellitus type II or in a pre-diabetic status.

NCT ID: NCT02672878 Not yet recruiting - Clinical trials for Coronary In-stent Restenosis

Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI)

RIBS VI
Start date: April 2014
Phase: Phase 4
Study type: Interventional

Treatment of patients with in-stent restenosis (ISR) remains a challenge. This study will assess the efficacy of Bioresorbable Vascular Scaffolds (BVS) (Abbott Vascular) in the treatment of patients suffering from ISR.