The Johns Hopkins Bayview Medical Center
Baltimore, Maryland, 21224, United States
NCT Number: NCT00685815
Double-blind, placebo-controlled, entitled: "Intravenous Iron Metabolism in Restless Legs Syndrome
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Baltimore, Maryland, 21224, United States
To determine the effects of high-dose infusions of iron on Restless Legs Syndrome (RLS) symptoms and brain concentrations of iron.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
500mg FCM in 250cc normal saline (NS) IV over one hour, once on Day 3, once on Day 4
Other names: Injectafer
250cc normal saline (NS) IV over one hour, once on Day 3, once on Day 4
Time frame: 2 weeks, 4 weeks, and 52 weeks
Number of weeks that patients were able to remain off treatment for RLS
American Regent, Inc.
Industry
Acronym: RLS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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