Status:
COMPLETED
Utility and Validation's Study of a Smartphone Application for Periodic Paralysis
Lead Sponsor:
Institut National de la Santé Et de la Recherche Médicale, France
Conditions:
Periodic Paralyses
Eligibility:
All Genders
12+ years
Brief Summary
Periodic paralyses (PP) are rare genetic disorders characterized by the occurrence of acute and reversible episodes of muscle weakness. Their episodic and highly variable nature makes it difficult to ...
Detailed Description
Primary periodic paralyses (PP) are rare autosomal dominant disease (estimated prevalence of one per 100.000 in Europe) due to mutations in genes encoding muscle ion channels. Symptoms usually start i...
Eligibility Criteria
Inclusion
- All patients with periodic paralysis aged over 12 years and followed in the National Channelopathies Reference Centre will be eligible for the study if they:
- are able to understand, read and write French
- are willing to and capable of entering their clinical and medico-social and economic data in the Smartphone application
- have an identified parent/caregiver for children aged 12-18 years (not mandatory for adults)
- are affiliated to a Health Insurance
- are able to give their informed consent (adult patients) or if their legal representatives are able to give their informed consent (child patients)
Exclusion
- Will not be eligible, patients
- with a condition that could explain hypokalemia: renal, adrenal, thyroid dysfunction, renal tubular acidosis, abuse of diuretic and laxative,
- with a condition that could explain hyperkalemia: renal, adrenal, thyroid dysfunction, use of potassium-sparing diuretics,
- who are under guardianship
Key Trial Info
Start Date :
July 25 2019
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 30 2024
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT05976958
Start Date
July 25 2019
End Date
December 30 2024
Last Update
January 30 2025
Active Locations (1)
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1
RaDiCo-PP
Paris, Île-de-France Region, France, 75012