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Syndrome clinical trials

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NCT ID: NCT03260348 Not yet recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome in Taiwan

Start date: September 1, 2017
Phase: N/A
Study type: Observational

The study enrolls ARDS patients in medical ICUs in 11 Hospitals in Taiwan. The epidemiology and long-term outcomes of the patients will be recorded.

NCT ID: NCT03252041 Not yet recruiting - Clinical trials for Pelvic Pain Syndrome

MRI & MRV in Pelvic Congestion Syndrome in Females

PCS
Start date: September 1, 2017
Phase: N/A
Study type: Observational

To investigate the feasibility of MRI and MRV in diagnosis of pelvic congestion syndrome.

NCT ID: NCT03235128 Not yet recruiting - Clinical trials for Nephrotic Syndrome Steroid-Resistant

Clinical Significance of Assesment of Serum miRNA-30a in Childhood Nephrotic Syndrome

Start date: October 1, 2017
Phase: N/A
Study type: Observational

Childhood nephrotic syndrome is the most frequent glomerular disease that presents during childhood,primarily owing to a disturbed immune function.This disease is characterized by alterations in selectivity at the glomerular capillary wall that lead to an inability to restrict the urinary loss of protein.

NCT ID: NCT03223454 Not yet recruiting - Asherman's Syndrome Clinical Trials

Human Amniotic Epithelial Cells for Asherman's Syndrome

Start date: October 2017
Phase: Phase 1
Study type: Interventional

This project aims to investigate the safety and effectiveness of human amniotic epithelial cells in the treatment of the severe refractory Asherman's syndrome.

NCT ID: NCT03222947 Not yet recruiting - Genetic Syndrome Clinical Trials

New Variants Involved in Taybi-Linder Syndrome

NewViTALS
Start date: September 2017
Phase: N/A
Study type: Observational

Taybi-Linder syndrome (TALS, OMIM 210710) is a rare autosomal recessive disorder belonging to the group of microcephalic osteodysplastic primordial dwarfisms (MOPD). This syndrome is characterized by short stature, skeletal anomalies, severe microcephaly with brain malformations and facial dysmorphism, and is caused by mutations in RNU4ATAC. Although RNU4ATAC-associated TALS is a recognizable phenotype, an atypical presentation is sometimes observed, thus expanding the clinical spectrum (TALS-like phenotype). This study aims to identify new variants involved in Taybi-Linder syndrome and associated phenotypes (i.e.TALS-like). This non interventional study will be performed on patients with no proven mutation of RNU4ATAC and their blood relatives (19 samples total) by high throughput sequencing and genetic analysis of already collected deoxyribonucleic acid samples. Altogether, such a study will allow a better understanding of the molecular mechanisms responsible for the Taybi-Linder syndrome and Taybi-Linder syndrome-like phenotypes as well as the pathophysiology of these devastating forms of microcephalic dwarfism.

NCT ID: NCT03222167 Not yet recruiting - Metabolic Syndrome Clinical Trials

Open-Label Efficacy and Safety Study of the Elbasvir/ Grazoprevir Fixed Dose Combination Patients With Chronic HCV GT1b

Start date: October 2017
Phase: Phase 3
Study type: Interventional

This is a multi-center, open-label trial of Elbasvir/ Grazoprevir 50/100 mg fixed dose combination 12 week treatment aimed to evaluate SVR12 in treatment naïve patients with chronic hepatitis C (genotype 1b) infection, associated with of metabolic syndrome. The study to be conducted in conformance with Good Clinical Practices. A total of 60 subjects will be studied at 2 sites in the Republic of Kazakhstan. Males and Females treatment naïve patients with CHC genotype 1b infection associated with metabolic syndrome (MS), 18-70 years of age, with or without severe fibrosis / compensated cirrhosis will be enrolled. SVR 12 (primary endpoint) will be evaluated. Patients will be stratified by fibrosis stage and presence of metabolic syndrome components. Interim Analysis will be performed in order to estimate viral kinetics, applicability of SVR4 and durability of SVR12 by evaluation of virologic response at week 4 and 8 of treatment and follow-up at week 4 (SVR 4) and 24 will be performed - this will be a descriptive summary only without hypothesis testing. The main hypothesis is that 12-week therapy with MK-5172 in combination with MK-8742 for treatment-naïve patients with HCV genotype 1b with metabolic syndrome is not notably worse than the same course for treatment-naïve patients with HCV genotype 1b without metabolic syndrome.

NCT ID: NCT03219684 Not yet recruiting - Clinical trials for Steroid Dependent and Steroid Resistent Nephrotic Syndrome

Cyclosporin A Therapy in Childhood Nephrotic Syndrome

Start date: April 1, 2018
Phase: N/A
Study type: Observational

Nephrotic syndrome (NS) is among the most common pediatric kidney diseases and is defined as massive proteinuria (>40 mg/m2/h or urine protein to creatinine ratio >2 g/g) leading to hypoalbuminemia (<2.5 g/dL), edema, and hyperlipidemia. 60-70 % of patients present prior to age of 6 years

NCT ID: NCT03140111 Not yet recruiting - Dry Eye Syndromes Clinical Trials

LAMELLEYE for the Treatment of Dry Eye Symptoms in pSS Patients

Start date: October 16, 2017
Phase: N/A
Study type: Interventional

Single-blind, randomised, single centre, 2-way crossover pilot study to investigate the effectiveness of LAMELLEYE for the treatment of dry eye symptoms in patients with primary Sjögren's Syndrome.

NCT ID: NCT03126383 Not yet recruiting - Clinical trials for Primary Sjögren Syndrome

Inflammatory Myopathies in Primary Sjögren's Syndrome

AMISS
Start date: May 10, 2017
Phase: N/A
Study type: Observational

The AMISS study will characterize the features of muscle disease in patients with primary Sjogren's syndrome (pSS).

NCT ID: NCT03088215 Not yet recruiting - Fibromyalgia Clinical Trials

Shock-Waves to Treat Fibromyalgia Pain

SWPW-FPS
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

Fibromyalgia pain syndrome is a common debilitating condition which associates mainly generalised pain, emotional distress and cognitive symptoms. The etiology is unknown, and no specific treatment exists so far. Lately, shock-waves have been used successfully to treat painful skeletal muscle, tendons and fascia, the investigators therefore hypothesize that shock-waves could be useful in alleviating Fibromyalgia pain. Two similar groups of participants bearing the condition will be prospectively compared. The first group will benefit from the application of shock-waves weekly for 12 weeks, the second will not. The investigators intend to study if there is any difference in pain and quality of life between the two groups at the end of the three months.