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Syndrome clinical trials

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NCT ID: NCT01111071 Completed - Clinical trials for Acute Coronary Syndrome

Variation Between Hospitals in Short-term Mortality After Acute Coronary Syndromes: A CALIBER Study

Start date: April 2010
Phase: N/A
Study type: Observational

We seek to investigate whether hospitals in England and Wales vary in their rate of mortality following admission for heart attack or unstable angina, the extent of such variation, whether discharge diagnosis affects the extent of variation, and whether such variation has changed over time. Furthermore, we will investigate what individual- or hospital-level factors explain variation in mortality between hospitals.

NCT ID: NCT01110642 Withdrawn - CHILD Syndrome Clinical Trials

Novel Treatment for Syndromic Ichthyoses

Start date: July 2011
Phase: Phase 2
Study type: Interventional

This is an open label-pilot study to assess the efficacy and safety of a novel cholesterol-lovastatin topical solution in children with rare syndromic ichthyoses. Often times, these children have difficulty in finding easily applied treatments to make their psoriasiform and ichthyotic plaques more manageable. We propose the use of a cholesterol-lovastatin topical solution as a treatment option with the hypothesis that it will lead to regression of involved areas and decreased erythema and warty-like appearance of the plaques. We plan to enroll children with syndromic ichthyoses over the age of 1 year for a 12 month study with a total of 5 visits and 5 phone calls.

NCT ID: NCT01109901 Completed - Clinical trials for Cubital Tunnel Syndrome

Comparison of Effect of Anterior Subcutaneous and Submuscular Transposition on Cubital Tunnel Syndrome

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine which surgical method is better for cubital tunnel syndrome in outcomes.

NCT ID: NCT01109706 Completed - Clinical trials for Acute Coronary Syndrome

Relevance of Plasma PCSK9 Concentration as a Biomarker in Acute Coronary Syndrome.

PC-SCA-9
Start date: February 13, 2011
Phase:
Study type: Observational

PCSK9 (Proprotein convertase subtilisin kexin type 9) plays a key role in LDL-cholesterol (LDLC) metabolism by inhibiting LDL receptor (LDLR) at post-transcriptional level. PCSK9 loss of function mutations are associated to decreased LDLC levels and a cardiovascular protection. In this context, the development of pharmacological inhibitors of PCSK9, in association with statins treatment, represents a major therapeutic issue for LDLC modulation. It was previously shown that PCSK9 plasmatic concentration correlated with plasmatic LDLC, TG and glucose concentrations. However, no data are available on predictive value of PCSK9 plasmatic level concerning coronary disease severity. The main objective of this study is to determine whether plasmatic PCSK9 concentration is linked to coronary damage severity in patients with acute coronary syndrome.

NCT ID: NCT01109537 Completed - Clinical trials for Restless Legs Syndrome

Altered Brain GABA and Glutamate in Restless Legs Syndrome

RLS
Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of the study is to understand the brain chemistry of people with Restless Legs Syndrome (RLS). The primary hypothesis is that patients with RLS will have reduced GABA levels in their Thalamus and elevated Glutamate levels in their Anterior Cingulate Cortex. The study will use MRS imaging to examine the regional levels of these neurochemicals, GABA and Glutamate, in the brain.

NCT ID: NCT01108549 Completed - Fibromyalgia Clinical Trials

Treatment of Chronic Fatigue Syndrome and Fibromyalgia With D-ribose- a Multicenter Study

Start date: April 2009
Phase: N/A
Study type: Interventional

To determine whether adding Ribose 5 grams 3 x day would improve quality of life, energy, sleep and cognitive function and decrease pain in patients with CFS and/or fibromyalgia (CFS/FMS).

NCT ID: NCT01107977 Completed - Clinical trials for Irritable Bowel Syndrome

Iyengar Yoga for Young People With Irritable Bowel Syndrome

Start date: January 2010
Phase: N/A
Study type: Interventional

Irritable bowel syndrome (IBS) affects as many as 14% of high school-aged students. Symptoms include discomfort in the abdomen, along with diarrhea and/or constipation and other gastroenterological symptoms, which can significantly impact quality of life and daily functioning of patients. Emotional stress appears to exacerbate IBS symptoms suggesting that mind-body interventions reducing arousal may prove beneficial. Often symptoms can be traced to childhood and adolescence, making the early manifestation of IBS important to understand. The current study focuses on young people aged 14-26 years of age with IBS. The study will test the potential benefits of Iyengar yoga (IY) on clinical symptoms, psychospiritual functioning and visceral sensitivity. Yoga is thought to bring physical, psychological and spiritual benefits to practitioners and has been associated with reduced stress and pain. Through its focus on restoration and use of props, IY is especially designed to decrease arousal and promote psychospiritual resources in physically compromised individuals. Sixty-four IBS patients aged 14-26 will be randomly assigned to a standardized 6-week biweekly IY group-based program (1.5 hour sessions) or a wait-list usual care control group. The groups will be compared on the primary clinical outcomes of IBS symptoms, quality of life and global improvement at post-treatment and 2 month follow-up. Secondary outcomes will include visceral pain sensitivity assessed with a standardized laboratory task (water load task), and psychospiritual variables including coping, self-efficacy, mood, acceptance and mindfulness. It is hypothesized that IY will be safe and feasible: with less than 20% attrition; and the IY group will demonstrate significantly improved outcomes compared to controls, with physiological and psychospiritual mechanisms contributing to improvements; clinical treatment gains will be maintained at 2 months following yoga.

NCT ID: NCT01107964 Completed - Dry Eye Syndrome Clinical Trials

Oral Omega-3 Fatty Acids in the Treatment of Dry Eye Syndrome

Start date: July 2010
Phase: N/A
Study type: Interventional

The investigators hypothesize that oral omega-3-acid ethyl esters (Lovaza, GlaxoSmithKline, Research Triangle Park, NC) will decrease dry-eye related symptoms as well as clinical markers associated with dry eye disease (Schirmer-1 test values, positive vital staining with lissamine green, and fluorescein tear break-up time) when compared to administration of placebo.

NCT ID: NCT01107899 Terminated - Clinical trials for Acute Coronary Syndromes

Study to Learn When Platelets Return to Normal After One Loading Dose of Anti-platelet Drugs in Patients With Symptoms of Acute Coronary Syndromes

Start date: October 2009
Phase: Phase 1
Study type: Interventional

To investigate how platelets recover to normal function in subjects who have symptoms of a heart attack or unstable angina and who get a loading dose of prasugrel or clopidogrel for planned coronary angiography.

NCT ID: NCT01107795 Terminated - Clinical trials for Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS)

Prospective Study to Evaluate Outcomes From Transoral BOT Resection for OSAHS

Start date: March 4, 2010
Phase:
Study type: Observational

This is a prospective observational study that will collect outcome data for patients who choose to undergo transoral tongue base operations for Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS)as part of their standard of care treatment. This is a data collection study only and does not provide for evaluations or treatment of OSAHS.