Comment Period Extended to 3/23/2015 for Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials
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4 studies found for:    Familial Periodic Paralyses

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Familial Periodic Paralyses
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Show studies first received on any dateShow studies that were first received in the last 14 days
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Rank Status Study
1 Completed
Has Results 		Hyper- and Hypokalemic Periodic Paralysis Study
Conditions: Hyperkalemic Periodic Paralysis;   Hypokalemic Periodic Paralysis
Interventions: Drug: Dichlorphenamide (double-blind);   Drug: Placebo (double-blind);   Drug: Dichlorphenamide (open-label)
2 Completed Phase III Randomized, Double-Blind, Placebo-Controlled Study of Dichlorphenamide for Periodic Paralyses and Associated Sodium Channel Disorders
Conditions: Paralysis, Hyperkalemic Periodic;   Hypokalemic Periodic Paralysis;   Paramyotonia Congenita
Intervention: Drug: dichlorphenamide
3 Recruiting Lamotrigine as Treatment of Myotonia
Conditions: Dystrophia Myotonica Type 1;   Myotonia Congenita;   Paramyotonia Congenita;   Hyperkalemic Periodic Paralysis;   Potassium-Aggravated Myotonia
Interventions: Drug: Lamotrigine;   Drug: Placebo
4 Active, not recruiting Genetic and Morphological Analysis of Thyrotoxic Periodic Paralysis
Condition: Thyrotoxic Periodic Paralysis
Intervention: Other: No intervention involved
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† Indicates status has not been verified in more than two years