Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:07 AM
Ignite Modification Date:
2025-12-25 @ 12:07 AM
NCT ID:
NCT05976958
Eligibility Criteria:
Inclusion Criteria:
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 Criteria: 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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
12 Years
Study:
NCT05976958
Study Brief:
Protocol Section:
NCT05976958