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Syndrome clinical trials

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NCT ID: NCT03767660 Recruiting - Venous Malformation Clinical Trials

Efficacy of Rapamycin (Sirolimus) in the Treatment of BRBNS, Hereditary or Sporadic Venous Malformation

Start date: July 31, 2018
Phase: Phase 4
Study type: Interventional

A prospective, nonrandomized, open-label, single-arm clinical trial to study efficacy of rapamycin (sirolimus) in the treatment of Blue Rubber Bleb Nevus Syndrome, hereditary or sporadic venous malformation

NCT ID: NCT03767439 Withdrawn - Clinical trials for Basal Cell Nevus Syndrome

Nivolumab With Vismodegib in Patients With Basal Cell Nevus Syndrome

Start date: July 2019
Phase: Phase 2
Study type: Interventional

This is a single-arm, phase II study to assess the efficacy of combined SMO and PD-1 inhibition with Vismodegib (SMO inhibitor) and Nivolumab (anti-PD-1 antibody) in BCNS patients (target enrollment of 22 patients), with a primary endpoint of 18-month disease control rate. The purpose of this study is to test the hypothesis that Nivolumab and Vismodegib will improve the percentage of BCNS patients who achieve disease control (defined as total tumor burden <50% of baseline) at 18 months from 50% to 80%. Baseline and on-treatment biopsies will be obtained to characterize the immune effects of combined SMO and PD-1 inhibition.

NCT ID: NCT03766542 Not yet recruiting - Overlap Syndrome Clinical Trials

Continuous Positive Pressure Versus Bi-level in Overlap Syndrome

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

Continuous positive airway pressure (CPAP) became the established treatment for overlap syndrome (OS). It has been showed that the survival benefits of CPAP favored hypercapnic patients. When considering hypercapnic stable COPD patients, survival benefits occurred when the use of bi- level ventilation therapy was targeted to significantly reduce hypercapnia. This highlights the relevance of hypercapnia and hypoventilation correction. Thus, the purpose of this study is to compare the use of CPAP to Bi-level ventilation in hypercapnic OS patients, since the later may correct not only the airway patency but also increase the magnitude of each breath.

NCT ID: NCT03765905 Completed - Clinical trials for Polycystic Ovary Syndrome

Evaluation of Serum Scube-1 Scube-2 and Scube-3 Levels in Patients With Polikistik Over Syndrome ,

Start date: December 1, 2017
Phase:
Study type: Observational

The aim of this study is to investigate serum SCUBE-1 and SCUBE-3 levels in PCOS and non-PCOS cases compared with non-PCOS healthy controls with similar age and body mass index

NCT ID: NCT03765593 Not yet recruiting - Clinical trials for Lymphoma, Non-Hodgkin

Biomarkers in Primary Sjögren's Syndrome

pSS
Start date: March 2019
Phase:
Study type: Observational

The clinical spectrum of primary Sjogren Syndrome (pSS)ranges from sicca syndrome to systemic involvement (extraglandular manifestations), including a large number of manifestations that may be the form of presentation or appear after the disease is diagnosed, and that clearly mark the prognosis of the disease. Gene expression levels of Interferon (INF) and B Lymphocyte Biomarkers as Markers of Systemic Affectation and Lymphoproliferative Disease in, together with clinical and laboratory parameters, will provide significant information about the risk of developing hematological neoplasms in patients with pSS at different stages of the disease, and lead to better management of the disease treatment and therapeutic behaviors. Using the proposed technique allows us to study the gene expression at the mRNA level of each biomarker, which allows us to anticipate the irreversible changes that take place due to the progress of the pathology in progress, since the molecular changes precede the histological changes and in the pathological diagnosis.

NCT ID: NCT03765463 Completed - Clinical trials for Tourette Syndrome in Adolescence

Extinction Learning in Youth With Tourette Syndrome

Start date: February 28, 2019
Phase: N/A
Study type: Interventional

Aversive sensory phenomena such as premonitory urges play a central role in the behavioral treatment model of tics. Extinction learning and extinction recall are learning processes implicated within this model, but have not been directly evaluated in youth with Tourette syndrome (TS). This study examines extinction learning and extinction recall in youth with TS using an experimental task. This study will also explore the relationship between extinction processes (i.e., extinction learning and extinction recall) and treatment outcomes with behavior therapy. Findings from this investigation will be used to update the behavioral treatment model, which serves as the basis for evidence-based behavioral interventions.

NCT ID: NCT03764761 Terminated - Down Syndrome Clinical Trials

Storybook Reading in Individuals With Down Syndrome

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

This study uses mobile eye-tracking technology in order to characterize patterns of visual attention to communication supports, as well as a partner, within real world interactions for individuals with Down syndrome. Visual communication supports are central components of what is termed augmentative and alternative communication (AAC) intervention. AAC refers to the methods and technology designed to supplement spoken communication for people with limited speech. "Aided" AAC is a subcategory in which an external aid stores and presents for use visual symbols such as photographs, line drawings, or alphabet letters. The most traditional means of structuring aided AAC displays is to present the language concepts within row-column grids, which contain individual symbols/concepts placed in each grid square. The investigator's previous work investigated whether these grid-based presentations could be improved by understanding how different perceptual features of the displays influence responding (i.e., whether what the display looks like influences how easily the information on it is found). Individuals with developmental disabilities and children developing typically were faster and more accurate in finding information on some displays over others, when tested using a "visual search" task (aka, a "finding game" - "find the dog"). The previous investigations have evaluated visual attention within a setting that isolated visual processing of the AAC display as the primary dependent measure. However, communication requires attention not only to an AAC display, but also to a communication partner. Therefore, the current study seeks to examine questions of visual attention to both an AAC display and a communication partner. The investigators will manipulate characteristics of the structure of the display (e.g., arrangement of symbols), in order to determine if more optimal displays facilitate desirable patterns of visual attention to both the communication display and the partner. The mobile eye-tracking technology captures attention to both the display and the communication partner. The investigators anticipate that participants will be able to attend to their partner and the shared activity more when the AAC display is more optimal, but that when the AAC display is sub-optimal, the participants will have to spend more time examining the AAC display and less time in actual communication.

NCT ID: NCT03764748 Recruiting - Tourette Syndrome Clinical Trials

Selective Microbiota Transplantation for Tourette's Syndrome

mini-FMT
Start date: April 17, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This study aimed to evaluate the role of selective microbiota transplantation on Tourette's syndrome (TS).

NCT ID: NCT03764735 Completed - Dry Eye Syndrome Clinical Trials

Study of SkQ1 as Treatment for Dry-eye Syndrome

VISTA-1
Start date: December 6, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether SkQ1 ophthalmic solutions are safe and effective compared to placebo for the treatment of the signs and symptoms of dry eye syndrome.

NCT ID: NCT03764592 Recruiting - Brugada Syndrome Clinical Trials

VF Mapping in Brugada and Early Repolarization Syndromes

Start date: February 23, 2018
Phase:
Study type: Observational

To determine the values and limitations of ECGI in guiding ablation and risk stratification in patients with BrS and Early Repolarization.