Genetic and Morphological Analysis of Thyrotoxic Periodic Paralysis
NCT ID: NCT02287363
Last Updated: 2014-11-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
160 participants
OBSERVATIONAL
2014-10-31
2017-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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TPP group
TPP patients(between episodes of paralysis), the inclusion criteria consisted of a certain history of acute limb muscle weakness, hypokalemia and decreased TSH with elevated free FT4, FT3. Subjects who suffered from hyperthyroid myopathy with long term muscle weakness, family periodic paralysis, renal tubular acidosis, hyperaldosteronism, hemiplegia, paraplegia, or any history of other metabolic or traumatic muscular disease were excluded.
No intervention involved
No interventions will be involved since it is an observational study
hyperthyroidism group
Control group, we included subjects with evidence of aberrant thyroid function (decreased TSH, elevated FT4, FT3) without paralysis. Graves' disease(GD) was preferred which required information concerning either increased thyrotrophin receptor antibody(TRAb) level, ophthalmopathy or diffusively enlarged goiter. Individuals with pure thyroid associated ophthalmopathy, history of thyroidectomy due to malignancy or adenoma as well as subacute thyroiditis and pituitary hyperthyroidism were excluded.
No intervention involved
No interventions will be involved since it is an observational study
Interventions
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No intervention involved
No interventions will be involved since it is an observational study
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
20 Years
60 Years
MALE
No
Sponsors
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West China Hospital
OTHER
Responsible Party
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Haoming Tian
professor
Principal Investigators
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Haoming Tian, MD.
Role: PRINCIPAL_INVESTIGATOR
West China Hospital
Other Identifiers
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HTian
Identifier Type: -
Identifier Source: org_study_id