Clin2
NCT06524726Likely a fitRecruiting

PNH registry for people with confirmed PNH

Paroxysmal Nocturnal Hemoglobinuria

Part of Blood & lymphatic, Kidney & urinary, Women’s health & pregnancy clinical trials.

This is a long-term registry study for people with a confirmed diagnosis of paroxysmal nocturnal hemoglobinuria (PNH). It simply collects information over time to better understand the condition and how it's managed. There is no experimental treatment involved.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
2,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You must have a confirmed diagnosis of PNH through a special blood test (flow cytometry).
  • You or your legal guardian must agree to take part and sign a consent form.
  • You cannot be currently enrolled in another interventional PNH clinical trial (but you may join later if you leave that trial).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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