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NCT ID: NCT03632629 Not yet recruiting - Clinical trials for Attention Deficit Hyperactivity Disorder

Effects of Cognitive Training on Children With Attention Deficit Hyperactivity Disorder

Start date: August 2018
Phase: N/A
Study type: Interventional

Using a single blind, randomized controlled design to study the additional therapeutic effects of cognitive training on traditional rehabilitation programs for children with attention deficit hyperactivity disorder and developmental delays.

NCT ID: NCT03629639 Not yet recruiting - Clinical trials for Psoriasis Vulgaris With Metabolic Disorders

Metformin for Treatment of Psoriasis Combined With Disorders of Glucose and Lipid Metabolism

MPGLM
Start date: September 1, 2018
Phase: Phase 4
Study type: Interventional

Psoriasis and metabolic disorders are well-known mutual comorbidities. The investigators hypothesized metformin can ameliorate both psoriasis and metabolic disorders mainly via gut microbiota modulation. The investigators design a randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of treatment of metformin for psoriasis combined with disorders of glucose and lipid metabolism and to explore the role of gut microbiota during the process.

NCT ID: NCT03613051 Not yet recruiting - Movement Disorders Clinical Trials

Assessment of Movement Skills in Autism Spectrum Disorder

Start date: April 1, 2019
Phase:
Study type: Observational

this study is to explore the degree of impairement in movement skills in children with autistic spectrum disorders

NCT ID: NCT03610529 Not yet recruiting - Unstable Angina Clinical Trials

CardioSenseSystem Compared Study Regarding Efficacy and Safety in the Monitoring of ECG

Start date: September 2020
Phase: N/A
Study type: Interventional

This is a prospective, controlled, comparative clinical trial of a new ECG monitoring system CardioSenseSystem prior CE marking. The aim of the study is to demonstrate that the CardioSenseSystem's cable-free ECG monitoring system (investigational device) is equivalent or better than traditional and accepted industry standard for cable-based ECG monitoring system (control device). In this study accepted industry standard is Philips Intellivue. In order to investigate this, the study will measure ECG monitoring interruptions, management time and alarm performance. The study population will consist of sixty (60) adult subjects requiring ECG and that are fulfilling the eligibility criteria for study participation. The subjects will be using both the investigational device and the control device simultaneous for measuring data loss, management time and alarm function up to 24 hours.

NCT ID: NCT03608449 Not yet recruiting - Anxiety Disorder Clinical Trials

Doing More With Less": Optimizing Psychotherapeutic Services in the Mental Health System

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Psychotherapy is one of the cornerstones of mental health services. It is provided by psychiatrist, psychologists and psychiatric social worker in both hospital and out-patient services, and is assumed to require massive manpower and training inputs. Internationally, the clinical outcomes of routine mental health services are rarely recorded or reported. However, a rough estimation is that half (40-60%) of all psychotherapies have a favorable clinical outcome. Recently (Clark et al, 2017), the English Improving Access to Psychological Therapies (IAPT) Program, which delivers psychotherapies to more than 537 000 patients in the UK each year, indicated that 44% of the patients recovered, and 62%- improved. Consistent with a causal model, most organizational factors also predicted between-year changes in outcome, together accounting for 33% of variance in reliable improvement and 22% for reliable recovery. The proposed study aims at dramatically improving the yield of psychotherapies in the Mental Health Services by combining monitoring and patient-therapist matching strategies. The first will be achieved by implementing Routine Outcome Monitoring (ROM), and the second- by applying a patient-therapist match-re-match procedure during psychotherapy

NCT ID: NCT03562104 Not yet recruiting - Clinical trials for Traumatic Brain Injury

Swallowing Disorders in Minimally Consciousness Patients (MCS)

TC-DEG
Start date: September 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to characterize swallowing disorders in minimally consciousness patients after brain traumatic injury.

NCT ID: NCT03519035 Not yet recruiting - Clinical trials for Borderline Personality Disorder

Study of Hallucinations in Patients With Borderline Personality Disorder

Start date: July 2018
Phase:
Study type: Observational [Patient Registry]

Hallucinations in borderline personality disorder are a frequent an serious trouble which have an important impact in patients lives. Despite this, they are often ignored by nursing staff, and are not an important criteria in Diagnostic and Statistical Manual (DSM) 5 and Classification Internationale des maladies (CIM-10). The main objective of our study is to assess the prevalence of this trouble in borderline personality disorder (BPD) population, and to characterize the hallucinations in order to compare our results with those of international studies.

NCT ID: NCT03510533 Not yet recruiting - Eating Disorder Clinical Trials

Validation of the Concept of the Autoantibodies Directed Against the Neuropeptides Involved in Food Intake Regulation on the Incidental Cases of Eating Disorders

EDILS-AutoAC
Start date: May 2018
Phase: N/A
Study type: Interventional

This study should lead to the validation of the concept of the autoAc directed against the neuropeptides involved in food intake regulation.

NCT ID: NCT03507985 Not yet recruiting - Memory Disorders Clinical Trials

Attention and Memory Disorders Related to Acute Morphine

MEMOMORPH
Start date: September 2018
Phase:
Study type: Observational

The aim of the study is to determine if there are attention disorders related to acute morphine use in single-traumatized patients and after that the investigators will determine whether there are immediate memory problems associated with acute morphine withdrawal in single-traumatized patients. From a biochemical point of view, the analgesic effects of morphine and the central side effects appear to be two different dimensions of the action of morphine, each related to a metabolite. Regarding acute attention, it is difficult to differentiate attention deficit disorder due to pain or due to morphine. Two tests have been validated in the literature to evaluate attention and memory: the 15 words of Rey and the Stroop Color Word test. The investigators will use these two tests in this study.

NCT ID: NCT03444740 Not yet recruiting - Clinical trials for Lower Urinary Tract Symptoms

Lower Urinary Tract Symptoms in Women and Adjustment Disorder

LUTS and AD
Start date: March 2018
Phase: N/A
Study type: Observational

Our hypothesis that the prevalence of AD in uro-gynecologic patients with LUTS who are seeking medical help for their condition is higher than that of the general population (indicated by high scores at the ADNM-20; score above 48). Taking into consideration that affective disorders, anxiety and depression among patients with LUTS present with a prevalence of 17-23% [20] as well as through long personal experience, we hypothesize that the prevalence of AD in this group is 20%.