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Primary hyperoxaluria

MONDO:0002474

A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.

Also known as: hyperoxaluria, primary, primary hyperoxaluria

17 clinical trials for this condition and its sub-types, 13 tagged with Primary hyperoxaluria itself.

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Part of

↑ Inborn carbohydrate metabolic disorder (370)

Sub-types of Primary hyperoxaluria

  • Primary hyperoxaluria type 1 10 trials
  • Primary hyperoxaluria type 2 4 trials
  • Primary hyperoxaluria type 3 2 trials
Including sub-types (17) Tagged with Primary hyperoxaluria (13)
Trials to join now! 9 Not yet recruiting 1 Completed 3
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  • New blood test could help kidney patients in israel

    Knowledge-focused Not yet recruiting

    This study aims to validate a blood test for measuring oxalate levels, which is currently not available in Israel. Researchers will compare results from a local lab with an external lab using 50 blood samples. They will also explore how vitamin C levels relate to oxalate in patie…

    Sponsor: Western Galilee Hospital-Nahariya • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:30 UTC

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