PMMHRI - Familial Hypercholesterolemia Registry

Recruiting now

Conditions studied: Familial Hypercholesterolemia

In brief

The registry is maintained at the Regional Centre for Rare Diseases, established in 2016, within Polish Mother's Memorial Hospital Research Institute. This facility diagnoses and treats over 80 distinct rare diseases in patients from across the country, including those with phenotypically or genetically confirmed familial hypercholesterolemia (FH).

Key facts

Study ID
NCT06571630
Run by
Polish Mother Memorial Hospital Research Institute
People needed
300
Starts
2018-01-01
Expected to finish
2025-12-31
Last updated by the study team
2024-08-26

Who can join

Age: 0 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Where it is running

Full record on ClinicalTrials.gov

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