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Restless Legs Syndrome clinical trials

View clinical trials related to Restless Legs Syndrome.

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NCT ID: NCT01192503 Terminated - Clinical trials for Restless Legs Syndrome

Safety and Efficacy of Rasagiline in Restless Legs Syndrome

RAS-RLS
Start date: September 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to find out if rasagiline improves RLS symptoms. We also want to make sure rasagiline is safe to give people with RLS.

NCT ID: NCT01174459 Completed - Clinical trials for Restless Legs Syndrome

Survey on Long-Term Use of BI-Sifrol® Tablets in Patients With Restless Legs Syndrome

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

The survey is conducted to investigate the safety and efficacy of long-term use of BI-Sifrol Tablets in Restless Legs Syndrome (RLS) patients with or without renal dysfunction in routine medical practice.

NCT ID: NCT01170091 Completed - Clinical trials for Restless Legs Syndrome

Safety and Effect of Mirapex(Pramipexole) Tablet Among Korean RLS

Start date: December 2007
Phase: N/A
Study type: Observational

Safety and Effect of Mirapex(Pramipexole) tablet among Korean Restless Legs Syndrome Patients: An Open-Label, Postmarketing Surveillance Study

NCT ID: NCT01138124 Completed - Hypertension Clinical Trials

Gabapentin and Risk of Pancreatic Cancer and Renal Cancer (GPRD)

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

High doses of gabapentin are associated with pancreatic acinar cell tumors in rats, but there has been no post marketing pancreatic carcinogenicity signal with gabapentin as reported by spontaneous reports in the Adverse Events Reporting System or in the published literature. In a published case-control screening study of the association of gabapentin with 55 cancers, the only cancer that met the screening criteria for possibly increased cancer risk with gabapentin exposure was renal (including renal pelvis) cancer. This association was judged to be likely due to or substantially accentuated by confounding by cigarette smoking, hypertension, and lifestyle (Cancer Causes Control 2009;20:1821-1835). The primary objective of this study is to determine whether exposure to gabapentin is associated with an increased risk of developing pancreatic cancer or renal cancer in the United Kingdom (UK) General Practice Research Database (GPRD). Almost all members of the UK population are registered with a General Practice, which centralizes the medical information not only from the general practitioners themselves but also from specialist referrals and hospital attendances. Over 487 General Practices contribute data to the GPRD. The study cohort from which cases and controls are drawn is all subjects in the GPRD 1993-2008. Gabapentin was approved in the UK in May 1993. Entry into the study cohort begins Jan 1, 1993 for all those who are registered in GPRD before that time, and at the time of registration if later than Jan 1, 1993. Patients with a first diagnosis of the respective cancer 1995-2008 are risk set matched with up to 10 controls within the same General Practice for age at cohort entry (within two years), sex, and year of entry into the study cohort (within one year). For cases, the index date is the date of first diagnosis of the respective cancer. The index date for controls is set as the date at which the follow-up time from cohort entry is the same as the case. The index date is chosen so as to give the control equal follow-up time to that of the case for ascertainment of use of gabapentin. Cases and controls will be required to have at least 2 years of follow-up in the study cohort before their index date. Data on gabapentin prescriptions are obtained for cases and controls from study cohort entry to the index date. Crude and adjusted odds ratios and 95% confidence intervals (CI) will be produced from conditional logistic regression models, with additional analyses evaluating for latency and dose-response. For pancreatic cancer, covariates are smoking, body mass index, diabetes, epilepsy, neuropathic pain, and chronic pancreatitis. For renal cancer, covariates are smoking, body mass index, diabetes, hypertension, diuretic use, epilepsy, and neuropathic pain.

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: NCT01061372 Withdrawn - Clinical trials for Restless Legs Syndrome

12-Week Efficacy And Safety Of Pregabalin In Treating Restless Legs Syndrome (RLS) Subjects

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

The purpose of this study is to assess efficacy and safety of pregabalin in treating moderate to severe Restless Legs Syndrome in comparison to placebo.