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Restless Legs Syndrome clinical trials

View clinical trials related to Restless Legs Syndrome.

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NCT ID: NCT01125033 Completed - Clinical trials for Kidney Failure, Chronic

Study of Vitamin C, Vitamin E and Their Combination to Treat Restless Legs Syndrome in Hemodialysis Patients

ShirazUMS
Start date: March 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether vitamin C, vitamin E and their combination are effective in the treatment of RLS in hemodialysis patients.

NCT ID: NCT01113710 Completed - Clinical trials for Idiopathic Restless Legs Syndrome

Non-interventional Study (NIS) in Patients With Restless Legs Syndrome in Daily Practise

RLS-Practise
Start date: May 2010
Phase: N/A
Study type: Observational

This non-interventional observational study is designed to gain data for Neupro® in restless legs syndrome (RLS) under real life conditions in line with the summary of product characteristics (SmPC) related to effectiveness, tolerability and switching practice from other dopaminergic drugs as well as titration schemes.

NCT ID: NCT01112644 Completed - Clinical trials for Moderate to Severe Idiopathic RLS With Daytime Symptoms

Oxycodone/Naloxone Prolonged Release (OXN PR) Compared to Placebo to Demonstrate Improvement in Symptoms of Restless Legs Syndrome (RLS) in Subjects With Moderate to Severe Idiopathic RLS With Daytime Symptoms

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

The primary objective for the 12-week Titration-/Maintenance Period is: To demonstrate superior efficacy of OXN PR compared to PLA in the improvement of symptom severity of RLS.

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: NCT01084551 Completed - Clinical trials for Idiopathic Restless Legs Syndrome

Study of SPM 962 in Patients With Restless Legs Syndrome (RLS)

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

The objective of this study is to evaluate the clinical efficacy and safety of SPM962 in patients with restless legs syndrome (RLS) with once-daily repeated doses of 4.5mg and 6.75mg during a 13-week dose-titration and maintenance period. This is a multi-center, randomized, placebo-controlled, double-blind, 3-armed parallel group comparison study. Efficacy will be determined by investigating the superiority of SPM962 to placebo in terms of the primary efficacy variable, change in International Restless Legs Syndrome Rating Scale (IRLS) total score from baseline to the end of the dose-maintenance period.

NCT ID: NCT00991276 Completed - Clinical trials for Restless Legs Syndrome

Polysomnography Study Of Pregabalin And Pramipexole Versus Placebo In Patients With Restless Legs Syndrome And Associated Sleep Disturbance

Start date: December 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of pregabalin and pramipexole versus placebo in the treatment of restless legs syndrome and associated sleep disturbance.

NCT ID: NCT00949858 Completed - Clinical trials for Obstructive Sleep Apnea

New Data Analysis Methods for Actigraphy in Sleep Medicine

Start date: July 2009
Phase: N/A
Study type: Observational

The purpose of this study is to develop statistical and informatics tools for analyzing and visualizing Acticalâ„¢ (actigraphy) data linked to fatigue in Sleep Medicine Center patients.

NCT ID: NCT00949806 Completed - Clinical trials for Restless Legs Syndrome

Restless Legs Syndrome Treatment With Botulinum Toxin

SOXIS
Start date: August 2009
Phase: Phase 2
Study type: Interventional

Restless Legs Syndrome (RLS) is a common sensori-motor disorder that causes sensory discomfort and motor restlessness, most often in the legs, which improves with movement. Although medications are available to treat the disorder, many people either experience side effects that prevent them from continuing on the medication or do not sufficiently respond to current RLS medications. Recently, botulinum toxin type A (BNT) has been reported to relief RLS in patients with severe symptoms but this was not confirmed by other anecdotal reports. The investigators propose to test the efficacy of BNT on RLS symptoms by designing a more controlled study. Ultimately, this may lead to extend the therapeutic arsenal of this disorder.

NCT ID: NCT00942253 Completed - Clinical trials for End Stage Renal Disease

Exercise Training in Dialysis Patients With Restless Legs Syndrome (RLS)

HDRLS
Start date: September 2006
Phase: Phase 2
Study type: Interventional

Uremic etiology Restless legs syndrome (RLS) has been associated with poorer quality of life (QoL) compared to RLS-free counterparts mainly due to sleep deprivation factors. Exercise training in hemodialysis (HD) patients with RLS has been proven to be a safe approach in temporally ameliorating RLS symptoms similarly to the use of pharmacological treatment with dopamine agonists. However it not known whether the exercise anabolic stimulus and the dopamine agonist treatment could act synergistically for the improvement of physical functioning and muscle performance as well as in the amelioration of augmentation symptoms in hemodialysis patients with RLS.

NCT ID: NCT00895232 Completed - Clinical trials for Restless Legs Syndrome

Iron Sucrose In The Treatment of Restless Legs Syndrome: Safety of Three Dose Regimens as Evaluated by Clinical Assessments

Start date: November 2003
Phase: Phase 2
Study type: Interventional

Non-randomized open label Phase II clinical trial in which subjects meeting criteria for RLS were assigned to 1 of 3 treatment cohorts. The first cohort received one 500 mg IV iron sucrose infusion in 500 mL normal sterile saline (NSS) administered over four hours. The second cohort received two 500 mg IV iron sucrose infusions in 500mL of NSS administered over four to six hours on two separate dates, separated by two to seven days. The third cohort received two 500 mg IV iron sucrose infusions in at least 500 mL of NSS over six hours within 30 hours of the start of the first infusion. Cohorts were enrolled and treated subsequently.