Clin2
NCT04257994Possibly a fitRecruiting

Study how heart cell connections differ in inherited rhythm problems

Arrhythmogenic Right Ventricular DysplasiaBrugada SyndromeCardiac Channelopathy

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

This study looks at how proteins that connect heart cells are distributed in people with inherited heart rhythm disorders (and some family members who may carry the gene). It aims to better understand the biology behind these conditions, which may help improve risk assessment and future care.

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

Phase
N/A
Enrollment
26 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older
  • You (or a close relative) are being seen for an inherited heart rhythm problem at St. George’s inherited heart clinic
  • You may be a person with symptoms, or a family member who carries the gene but may not have symptoms yet
  • You can have any treatment plan (medicines, devices, or procedures) and still join
  • You are able and willing to sign informed consent for the study
  • You can explain the study in English, or you have a translator available if needed

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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