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Syndrome clinical trials

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NCT ID: NCT04133129 Not yet recruiting - Obesity Clinical Trials

Effects of HIIT on Metabolic Syndrome

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

The project aims to find out the differences between two different types of structured training interventions have on the lipid profile of persons with diagnosed dyslipidemia. Each training intervention will last for 12 weeks. Subjects participating in the project will undergo a series of tests before and after the training intervention which will allow us to make conclusions.

NCT ID: NCT04120779 Not yet recruiting - Metabolic Syndrome Clinical Trials

Study Protocol of the EMPOWER-SUSTAIN Project

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

A pilot randomised controlled trial will be conducted in UiTM Primary Care Clinic, Selayang Campus, Selangor, Malaysia. A total of 232 patients with Metabolic Syndrome (MetS) will be recruited; 116 will be randomised to receive the EMPOWER-SUSTAIN intervention for 6 months and another 116 patients will continue with usual care. The EMPOWER-SUSTAIN intervention is a multifaceted chronic disease management strategies based on the Chronic Care Model (CCM) and persuasive technology theory. It consists of training physicians and patients to use the EMPOWER-SUSTAIN web-based self-management intervention mobile apps, strengthening patient-physician relationship and reinforcing the use of relevant clinical practice guidelines for management and prescribing. The primary outcome is the mean change in patient activation score using the Patient Activation Measure short form Malay version (PAM-13-M) questionnaire. The secondary outcomes include the change in patients' physical activity level, eating behavior, patients' perception on chronic illness care, satisfaction in physician-patient interaction and perceived absolute 10-year cardiovascular disease (CVD) risk.

NCT ID: NCT04119739 Not yet recruiting - Clinical trials for Carpal Tunnel Syndrome

Pain Reduction Produced by Different Treatments in Carpal Tunnel Syndrome

Start date: April 14, 2020
Phase: Phase 4
Study type: Interventional

Pain reduction effects of the median nerve neural mobilization technique (a physiotherapy treatment) will be compared to those produced by a pharmaceutical treatment and the absence of treatment, in subjects who suffer carpal tunnel syndrome.

NCT ID: NCT04104958 Not yet recruiting - Clinical trials for Polycystic Ovary Syndrome

IVF Outcome in Polycystic Ovary Syndrome Patients

Start date: March 1, 2020
Phase:
Study type: Observational

1. To investigate the circulating concentrations of phoenixin and their associations with BMI, the concentrations of sex hormones including (LH), (FSH), (E2), (P4), (TT) and steroid hormones enzyme in PCOS patients. 2. To detect the expression PNX and humanin in women with or without PCOS and to elucidate possible correlations with ovarian reserve and clinical outcomes after IVF-ICSI. 3. To investigate relationship between PNX, humanin expression and PI3K/AKT/mTOR and autophagy pathway as a major signaling mechanism in PCOS for targeting new prognostic and therapeutic markers. 4. The study investigates the correlation between oocyte maturity, fertilization, recent biomarkers and a variety of hormonal parameters in follicular fluid.

NCT ID: NCT04104620 Not yet recruiting - Clinical trials for Organ-specific Autoimmune Diseases

Autoimmunity in Patients With GAD-Ab and Their Relatives

FamilyGAD
Start date: September 30, 2019
Phase:
Study type: Observational [Patient Registry]

A group of poorly studied immune-mediated neurological syndromes are associated with antibodies against glutamic-acid decarboxylase (GAD-Ab). GAD is the rate-limiting enzyme for the synthesis of gamma aminobutyric acid (GABA) from glutamate and is expressed by inhibitory neurons of the central nervous system. Neurological syndromes with anti-GAD antibodies (GAD-Ab) are often non-paraneoplastic. They mainly include limbic encephalitis (LE), cerebellar ataxia (CA) and stiff-person syndrome (SPS). Although the pathogenic role of GAD-Ab is controversial, most patients have high serum levels and GAD-Ab are also detected in the cerebrospinal fluid (CSF) along with other inflammatory abnormalities such as oligoclonal bands. GAD-Ab may also be present in the serum of T1DM patients, as pancreatic beta cells also express GAD, but usually at much lower titers than those of neurological patients. Organ-specific autoimmune diseases, such as T1DM and autoimmune thyroid disease, are common among patients with GAD-Ab and neurological syndromes and in their relatives, suggesting a shared genetic predisposition to autoimmune disorders. This is also supported by family reports of neurological syndromes with GAD-Ab and some HLA associations described in SPS. The aim of this study is to describe the different autoimmune organ-specific diseases present in patients with GAD-Ab and their relatives, along with to identify families with higher aggregation of autoimmune diseases and establish potential ways of inheritability.

NCT ID: NCT04093440 Not yet recruiting - Metabolic Syndrome Clinical Trials

Cardiometabolic Syndrome Response to Therapeutic Lifestyle Changes

COSMETIC
Start date: October 2019
Phase: N/A
Study type: Interventional

Intensive lifestyle intervention has shown to be effective in high risk patient populations and has gathered support from leaders—as outlined in the 2015 consensus paper by the Cardiometabolic Health Alliance. Thus there has been a call to establish new care models that assist Metabolic Syndrome patients in reducing there risk. The investigators aim to evaluate the impact of a lifestyle intervention program on metabolic syndrome patients.

NCT ID: NCT04092140 Not yet recruiting - Clinical trials for Carpal Tunnel Syndrome

Neuromuscular Ultrasound in Correlation to Neurophysiological Findings

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

1. Study the neuromuscular ultrasound findings in different types of neuropathies 2. correlation between ultrasound and neurophysiological findings in peripheral nerve diseases 3. correlation between clinical pain scale and severity of neuropathy

NCT ID: NCT04092088 Not yet recruiting - Clinical trials for Carpal Tunnel Syndrome

Effects of Cerebral & Peripheral Electrical Stimulation on Pain and Function in CTS

DCS-ENS-CTS
Start date: December 2019
Phase: N/A
Study type: Interventional

This is a randomized, double-blind, multi-center, factorial clinical trial to study the effectiveness of cerebral and peripheral electrical stimulation on pain and functional limitations associated with carpal tunnel syndrome (CTS). The study subjects will be randomly into four groups; (1) active trans-cranial direct current stimulation (tDCS) + active trans-cutaneous electrical nerve stimulation (TENS), (2) active tDCS + sham TENS, (3) sham tDCS + active TENS and (4) sham tDCS + sham TENS. The patient will be assessed by Brief Pain Inventory (BPI), Beck Depression Inventory (BDI), The Douleur Neuropathique en 4 questions (DN4), Quantitative sensory testing (QST), Pain Pressure Test (PPT) with algometer, Conditioned pain modulation (CPM), Patient ratings of improvement, or worsening, of the pain condition, Quality of Life short-form (SF)-36, Visual Analog Mood Scale (VAMS), Mini Mental Status Exam (MMSE) and Adverse Events Questionnaire (AEs). This study aims to investigate whether cerebral and peripheral electrical stimulation combined are more effective in relieving pain and functional limitations than the separate application of electrical stimulation in patients with CTS.

NCT ID: NCT04074122 Not yet recruiting - Clinical trials for Ventricular Tachycardia

Electromechanical Profiling of the Long-QT Syndrome (LQTS)

EMLoQ
Start date: January 1, 2020
Phase:
Study type: Observational

High-resolution, non-invasive electromechanical mapping in genotyped long-QT syndrome patients and healthy controls at baseline and during smart provocation.

NCT ID: NCT04073173 Not yet recruiting - Clinical trials for Respiratory Distress Syndrome in Premature Infants

Stress Assessment With and Without Analgesia During Surfactant Therapy in Preterm Infants.

Start date: November 1, 2020
Phase: Phase 4
Study type: Interventional

This study will compare stress, changes in oxygenation and oxidative damage in preterm infants with respiratory distress syndrome (RDS) randomized to receive or not remifentanil as an analgesic drug during the administration of porcine surfactant (poractant alfa, Curosurf®) through the traditional (INSURE) or the less invasive (LISA) method.