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Syndrome clinical trials

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NCT ID: NCT01613495 Active, not recruiting - Clinical trials for Prader Willis Syndrome

Ghrelin Suppression by Octreotide in Prader-Willi

Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to learn more about how octreotide (Sandostatin LAR® Depot) affects levels of ghrelin, hunger, and body weight in people with Prader-Willi Syndrome.

NCT ID: NCT01613456 Completed - Clinical trials for Irritable Bowel Syndrome

Effect of Saccharomyces Cerevisiae on the Symptoms of Irritable Bowel Syndrome

Start date: December 2011
Phase: N/A
Study type: Interventional

The main purpose of this study is the effect of the probiotic yeast Saccharomyces cerevisiae CNCM I-3856 on abdominal pain or intestinal discomfort in patients presenting with the irritable bowel syndrome (IBS)

NCT ID: NCT01612364 Recruiting - Clinical trials for Complex Regional Pain Syndrome I of Upper Limb

RCT :Thoracic Sympathetic Block for the Treatment of Complex Regional Pain Syndrome I of the Upper Limb

Start date: January 2010
Phase: Phase 3
Study type: Interventional

This is a double-blind randomized controlled trial to evaluate the efficacy of the sympathetic block via thoracic vertebra T3 for the treatment of CRPS I upper limb. Patients with CRPS I refractory to medical treatment will be subjected to four physical therapy sessions and then the randomized for experimental or control block and then more four physiotherapy sessions. Patients will be evaluated after one month of the blockade (primary outcome) and then up to 12 months. Will be evaluated by analgesic scale (Mcgill, brief pain inventory, dn4 questionnaire, NPSI, VAS), functional (ADM) and quality of life (HAD and WHOQOL-brief).

NCT ID: NCT01609426 Completed - Clinical trials for Idiopathic Nephrotic Syndrome

Factors of Steroid Dependency in Idiopathic Nephrotic Syndrome

NEPHROVIR-2
Start date: September 2012
Phase: N/A
Study type: Observational

The primary purpose of the study is to identify the factors of steroid dependency in childhood idiopathic nephrotic syndrome. The steroid dependency is defined by a relapse of nephrotic syndrome within the 3 weeks that follow the withdrawal of steroid therapy after the first manifestation. Different clinical and biological factors will be analyzed: age of first manifestation, delay of remission, ethnicity, and preceding viral infection, geolocalization in the Parisian area, genoprevalence of herpes viruses and polymorphisms in the genes involved in the response to steroid therapy.

NCT ID: NCT01609166 Completed - Hand-foot Syndrome Clinical Trials

Effectiveness Allopurinol Topical Agent Prevention Capecitabine-induced Hand-foot Syndrome

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

Hand-foot syndrome (HFS) is a dose-limiting toxicity of capecitabine for which no effective preventative treatment has been definitively demonstrated. This trial is conducted on the basis of preliminary data that a 3% allopurinol-based topical agent may prevent HFS. A randomized, double-blind phase III trial will evaluate 40 patients receiving their first ever cycle of capecitabine at a dose of either 2,000 or 2,500 mg/m2 per day for 14 days. Patients will be randomly assigned to a 3% allopurinol versus a placebo cream, which will be applied to the hands and feet twice per day for 6 months after the start of capecitabine. Patients will be examined every month and the investigators will take some photographs of hands and feet. HFS toxicity grade (Common Terminology Criteria for Adverse Events [CTCAE]v3.0) will be also collected at baseline and at the end of each cycle. The primary end point is the incidence of moderate/severe HFS symptoms at the end of capecitabine treatment , based on the patient-reported dermatological exploration.

NCT ID: NCT01609062 Terminated - MPS IVA Clinical Trials

Safety and Exercise Study of Two Doses of BMN 110 for Morquio A Syndrome

Start date: April 2012
Phase: Phase 2
Study type: Interventional

The primary objective of this study was to evaluate the safety of a 2.0 mg/kg/week and a 4.0 mg/kg/week of BMN 110 in patients with Morquio A syndrome for up to 196 weeks. Secondary objectives were to investigate the effect of the two doses on exercise capacity for up to 196 weeks. In addition, the pharmacokinetic (PK) parameters of both doses of BMN 110 was assessed.

NCT ID: NCT01607320 Terminated - Clinical trials for Polycystic Ovarian Syndrome

Efficacy Study of Raloxifene to Induce Ovulation in Polycystic Ovarian Syndrome

PCOS
Start date: June 2012
Phase: N/A
Study type: Interventional

This study examines Raloxifene versus Clomiphene to induce ovulation in women with polycystic ovarian syndrome (PCOS).

NCT ID: NCT01607073 Completed - Dravet Syndrome Clinical Trials

Verapamil as Therapy for Children and Young Adults With Dravet Syndrome

Start date: April 2012
Phase: Phase 2
Study type: Interventional

This study will assess how well the drug verapamil can improve control of seizures and dysautonomia symptoms in children and young adults diagnosed with Dravet syndrome. The safety of verapamil when given with all concomitant medications will also be assessed.

NCT ID: NCT01605266 Recruiting - Nephrotic Syndrome Clinical Trials

INSIGHT (Insight Into Nephrotic Syndrome)

INSIGHT
Start date: January 2011
Phase:
Study type: Observational

INSIGHT is a longitudinal study of childhood nephrotic syndrome to determine genetic, serologic and environmental factors contributing to nephrotic syndrome and disease progression.

NCT ID: NCT01603446 Completed - MELAS Syndrome Clinical Trials

L-arginine Therapy on Endothelium-dependent Vasodilation & Mitochondrial Metabolism in MELAS Syndrome

Start date: May 2012
Phase: Phase 2
Study type: Interventional

MELAS patients suffer from exercise intolerance, weakness, poor vision or blindness, poor growth, developmental delay, and deafness. They also have unique 'stroke-like' episodes (SLEs) which are not due to blockages of large or medium arteries. These 'strokes' are thought to be due to energy failure of very small brain blood vessels combined with energy failure in the mitochondria (cell battery) of the brain cells, especially in the back region of the brain in the vision centre. This leads to visual loss and paralysis. The overall goal of this study is to better understand the mechanism of these SLEs at the level of the brain cells and small blood vessels.