Hereditary spherocytosis
MONDO:0019350Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.
Also known as: Minkowski-Chauffard disease, congenital spherocytic hemolytic anaemia, hereditary spherocytosis, spherocytic anaemia, congenital spherocytosis
11 clinical trials for this condition and its sub-types, 2 tagged with Hereditary spherocytosis itself.
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Sub-types of Hereditary spherocytosis
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Hereditary spherocytosis type 1 0 trials
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Hereditary spherocytosis type 2 0 trials
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Hereditary spherocytosis type 3 0 trials
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Hereditary spherocytosis type 4 0 trials
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Hereditary spherocytosis type 5 0 trials
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Smartwatch signals may flag anemia, no needle needed
Diagnosis Not yet recruitingAnemia often goes unnoticed because diagnosis requires a blood draw. This study tests whether a wrist-worn smartwatch can identify people likely to have anemia by tracking blood flow, heart rate, oxygen, and movement. About 400 adults, with and without anemia, will wear the watch…
Sponsor: Peking Union Medical College Hospital • Aim: Diagnosis
Last updated Sep 03, 2026 00:00 UTC
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Could a painless light sensor replace the needle for anemia screening?
Diagnosis Not yet recruitingThis study tests whether a non-invasive device that uses light to measure hemoglobin through the skin can accurately detect anemia. Researchers will compare its readings with standard blood tests in 150 adults in Jakarta. If the device proves reliable, it could offer a quick, pai…
Sponsor: Tarumanagara University • Aim: Diagnosis
Last updated Jul 17, 2026 00:00 UTC