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Active clinical trials for "Syndrome"

Results 9541-9550 of 9759

Post-trial Access Program of Idursulfase-IT Along With Elaprase in Children With Hunter Syndrome...

Hunter Syndrome

This post-trial access program is to allow continued access for people who participated and are benefitting from treatment on the HGT-HIT-046 (NCT01506141) or SHP609-302 (NCT02412787) studies, which will be closed down. Idursulfase-IT also known as TAK-609, is a medicine to help treat Hunter Syndrome and issues with remembering, learning new things, and concentrating, also called cognitive impairment.

Available4 enrollment criteria

Compassionate Use Protocol for the Treatment of Autoinflammatory Syndromes

Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy and Elevated Temperature (CANDLE)Juvenile Dermatomyositis (JDM)2 more

The Requesting Physician/Investigator contacts Lilly when, based on their medical opinion, a patient meets the criteria for inclusion in the expanded access program.

No longer available29 enrollment criteria

A Treatment Investigational New Drug (tIND) Program of Tegaserod in Women With Irritable Bowel Syndrome...

Irritable Bowel Syndrome With ConstipationChronic Idiopathic Constipation

To provide tegaserod to eligible women adult patients who did not have satisfactory improvement of their irritable bowel syndrome with constipation (IBS-C) or chronic idiopathic constipation (CIC) symptoms with other available treatment(s) and / or patients who had satisfactory improvement of their symptoms with prior tegaserod treatment for IBS-C or CIC.

No longer available16 enrollment criteria

Assessment of Subsynovial Connective Tissue Thickness in Carpal Tunnel Syndrome

Carpal Tunnel Syndrome

The general aim of this research is to gain insight in the role of SSCT in the etiology and progression of CTS. We hypothesize that (degenerative) damage of the SSCT occurs early on in the pathogenesis of CTS. Fibrotic damage to the SSCT will lead to altered morphology and biomechanical characteristics. This eventually may lead to damage of the median nerve. To examine the SSCT an ultrasound technique described by Van Doesburg et al. 2012 will be used First, the reliability of the US technique to characterize morphology of the SSCT will be investigated. Secondly, cross-sectional data will be collected in healthy subjects and CTS patients to provide descriptive parameters and to describe differences between patients and controls. In the final part a prospective study will be conducted to look at changes of SSCT thickness over time and after treatment.

Unknown status12 enrollment criteria

Use of Novel Plasma and Urinary Biomarkers to Predict the Development of Hepatorenal Syndrome in...

Hepatorenal Syndrome

This study investigated the use of novel plasma and urinary biomarkers to predicte the development of hepatorenal syndrome in patients with advanced cirrhosis. The biomarkers investigated include plasma cystatin C, plasma NGAL, plasma NAG, plasma IL-18, plasma ADMA, plasma BTP, urinary KIM-1 and urinary LFABP. These biomarkers will be checked in advanced cirrhotic patients who have or have not developed hepatorenal syndrome and compared between the two groups. These biomarkers will also be correlated with the occurence of hepatorenal syndrome.

Unknown status3 enrollment criteria

Women With Polycystic Ovary Syndrome (PCOS)

Polycystic Ovary Syndrome

Metabolic profile in women of different body composition with polycystic ovary syndrome.

Unknown status5 enrollment criteria

Saliva Cortisol Measurement as a Screening Test for Suspicious Cushings Syndrome in Children.

Cushings Syndrome

Cortisol overproduction ( Cushings syndrome) is a condition where the patient have a special fat distribution, with accumulation of fat around the abdomen and in the neck, with thinner limbs and weak musculature. The condition can be difficult to separate from adipositas in general. Screening for hypercortisolism in adults has been easier the last years, because we can measure free cortisol in saliva samples at late night. In children we still dont have reference ranges for saliva cortisol in children, so the screening is still troublesome, based on Collection of 24-hour urine.The meaning of this study is to establish reference ranges for saliva cortisol, and evaluate in a cohort with adipose children if screening with saliva cortisol is sensitive and specific enough to be the New screening test for hypercortisolism in children too.

Unknown status2 enrollment criteria

Microbiota Community of Irritable Bowel Syndrome in Episodes and Remission Phase

Irritable Bowel Syndrome

Analyze microbiota community of irritable bowel syndrome in episodes phase and remission phase.

Unknown status9 enrollment criteria

Clinical Study to Validate the Use of a New Point of Care Troponin I Test

Acute Coronary Syndrome

This trial is designed as a prospective, multi-center, observational study of "all-comers" eligible adult subjects presenting to participating emergency departments with symptoms suggestive of acute coronary syndrome (ACS)

Unknown status6 enrollment criteria

Clinical Decision Support System to Define 30 Day Adverse Clinical Events for Emergency Department...

Acute Coronary SyndromeClinical Decision Support System

Acute coronary syndromes are among main complains for patients presenting to emergency department. Risk classification systems are used to classify patients to appropriate risks and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.

Unknown status5 enrollment criteria
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