Clin2
NCT07474428Possibly a fitNot yet recruiting

Quality of life in young people with HHT

Hereditary Haemorrhagic Telangiectasia (HHT)

Part of Blood & lymphatic, Genetic & congenital, Heart & circulation clinical trials.

This study is about understanding how HHT (a condition that causes abnormal blood vessels) affects quality of life in children and young adults. If you join, you (or your caregiver) will fill out a survey about your daily life and symptoms.

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

Phase
N/A
Enrollment
70 people
Ages
2 years to 25 years
Study type
Observational

Who can take part

  • You must be between 2 and 25 years old.
  • You must have a confirmed diagnosis of HHT (hereditary hemorrhagic telangiectasia).
  • You must receive care at Cincinnati Children's Hospital HHT Center (at least one visit with a genetic counselor or the center director).
  • You must be able to complete a survey in English, or have a parent/guardian complete it for you if you are under 18.
  • If you are 8 to 17 years old, you must agree to take the survey (assent).

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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