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Syndrome clinical trials

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NCT ID: NCT03138473 Completed - Clinical trials for STEMI - ST Elevation Myocardial Infarction

Impact of Residual Syntax Score and Syntax Revascularization Index on Outcomes of ACS Patients With Multi-Vessel Disease

Start date: July 1, 2018
Phase:
Study type: Observational

The investigators want to assess the use of the residual SYNTAX score and the SYNTAX Revascularization Index as predictors for in-hospital outcomes and mid-term (6 months to 1 year) outcomes in patients with multi-vessel disease (MVD) who undergo PCI in the setting of STEMI or NSTEACS. Both values will be calculated in a number of patients over one year, and the relationship between both values and patient outcomes will be evaluated.

NCT ID: NCT03137472 Recruiting - Clinical trials for Complex Regional Pain Syndromes

TMS for Complex Regional Pain Syndrome

Start date: April 24, 2017
Phase: N/A
Study type: Interventional

The aim of the current study is to assess the efficacy of TMS in the treatment of Complex Regional Pain Syndrome (CRPS). It is hypothesized that participants who receive TMS (Group 1) relative to sham treatment (Group 2) once daily for two days will demonstrate a greater improvement in CRPS-related pain and other associated symptomology (i.e., cognitive, emotional and physical) compared to baseline. Participants will be followed until they reach their baseline for two consecutive weeks to assess safety and duration of symptom alleviation.

NCT ID: NCT03137355 Recruiting - Leigh Syndrome Clinical Trials

The International Registry for Leigh Syndrome

Start date: June 17, 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to develop a database containing clinical and laboratory information for patients with Leigh syndrome. The goal is to provide a greater understanding of Leigh syndrome allowing further characterization of this disease.

NCT ID: NCT03135821 Recruiting - Clinical trials for Irritable Bowel Syndrome

Traditional Chinese Medicine for Treatment of Irritable Bowel Syndrome

Start date: March 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Irritable bowel syndrome (IBS) is a prevalent condition that adversely affects patient's quality of life and represents a large health care burden globally. Currently, there is no satisfactory treatment for IBS and Chinese Herbal medicine (CHM) has been suggested to be potentially useful. However, the efficacy of CHM in the treatment of IBS is unclear and its mechanism of action is unknown. To date, attempts to characterize CHM efficacy universally suffer from poor scientific method or they do not faithfully replicate authentic CHM best practice. The overall goal of this proposal is hence to address these deficiencies by combining the best of CHM with western medicine.The investigators propose a 10-week randomized, double-blind, placebo-controlled study on 104 patients that form the intersect between western medicine and CHM. The participants would fulfill ROME III criteria for IBS-Constipation predominant subtype, which is also the TCM (Traditional Chinese Medicine) syndrome of Liver Qi stagnation. The investigators will test a core herbal formula specific for treatment of Liver Qi stagnation against placebo that consist of only 10% active ingredients but which is indistinguishable by taste from active treatment. Efficacy will be assessed by comparing symptoms reported at baseline (2-week run-in period) to end of treatment (8 weeks) and an optional follow up period (12 weeks). The primary end point will be improvement in IBS-Symptom Severity Score. Mechanism of action will be explored by measuring changes to the stool microbiome and GI transit times. If successful, this trial would provide one of the first evidence- and mechanism-based approach to translate CHM into mainstream IBS management.

NCT ID: NCT03135236 Completed - Down Syndrome Clinical Trials

Parents as the Primary Sexuality Educators for Their Young Adults With Down Syndrome

Start date: March 6, 2017
Phase: N/A
Study type: Interventional

By integrating sexuality and disability literatures, theories, and research methodologies, this study aims to: 1) contribute to the limited knowledge professionals have of parents as the primary sexuality educators; 2) create a resource for parents in order to be sexuality educators for their young adults with I/DD; and 3) evaluate the effectiveness of the Home B.A.S.E. for Developmental Disabilities Curriculum. In order to meet the objectives the study seeks to answer the following questions: 1. What is the effectiveness of a sexuality education workshop for parents of young adults with DS on improving the self-efficacy and attitudes around sexuality and healthy relationships for young adults with DS as well as increase the parent-child communication on sexuality topics? 2. What are parents' concerns that impact their ability to be the primary sexuality educators for their young adults with DS? It is proposed that parent confidence and comfort talking about sexuality topics with their young adult with Down syndrome will increase thereby increasing the parent-child communication as a result of this study.

NCT ID: NCT03134703 Terminated - Clinical trials for Neonatal Abstinence Syndrome

Methadone Demonstration Project With Neonatal Intensive Care Unit Infants Diagnosed With Neonatal Abstinence Syndrome

Start date: February 27, 2017
Phase: Phase 2
Study type: Interventional

This is a non-randomized, un-blinded feasibility study project comparing the Length of Stay (LOS) of Neonatal Intensive Care Unit (NICU) infants diagnosed with Neonatal Abstinence Syndrome (NAS) treated with methadone with historical data and a comparison group of NICU NAS infants treated with a different narcotic agent.

NCT ID: NCT03132935 Completed - Clinical trials for Acute Coronary Syndrome

Telemedical vs. Conventional Prehospital Care in Acute Coronary Syndromes

Start date: January 1, 2014
Phase: N/A
Study type: Observational

Telemedically supported paramedic care of acute coronary syndromes was compared to a historical control period of solely conventional on-scene physician care. Quality outcomes based on current guidelines were researched als well as time requirements in both groups.

NCT ID: NCT03132545 Completed - Clinical trials for Polycystic Ovary Syndrome

Resting Metabolic Rate, Fat Distribution, Endocrine and Metabolic Features in Polycystic Ovary Syndrome

Start date: January 2013
Phase: N/A
Study type: Observational

In a longitudinal, prospective and observational study, patients with PCOS and controls wore the SenseWear Armband for 2 days. Resting metabolic rati (kcal/die), total energy expenditure (MET, kcal) were evaluated. Ultrasonographic pelvic examinations, hirsutism score, anthropometric and menstrual pattern evaluation, hormonal profile assays, oral glucose tolerance test (OGTT) and lipid profile were performed.

NCT ID: NCT03132337 Completed - Clinical trials for Sinusoidal Obstruction Syndrome

Sinusoidal Obstruction Syndrome for Stem Cell Transplant Patients Biomarker Study

SOSBiomarker
Start date: April 1, 2017
Phase:
Study type: Observational

The goal of this is to learn more about stem cell transplant and complications that some people have after their transplants, in particular sinusoidal obstruction syndrome (SOS), also called veno-occlusive disease of the liver.

NCT ID: NCT03132051 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Sonographic Evaluation of Patients With Carpal Tunnel Syndrome Following Steroid Injection

Start date: April 2013
Phase: N/A
Study type: Interventional

The objective of this study was to assess sonographic changes of the median nerve after steroid injection for carpal tunnel syndrome.