Not Yet RecruitingPhase 4ACTRN12620000934943

Quinidine therapy in Brugada Syndrome

Investigating non-invasive markers to determine the effect of quinidine treatment in patients with Brugada Syndrome.


Sponsor

Sydney Local Health District

Enrollment

15 participants

Start Date

Oct 5, 2020

Study Type

Interventional

Conditions

Summary

Quinidine is the only drug shown to reduce the risk of dangerous irregular heart rhythms in Brugada Syndrome. While studies have shown invasive electrophysiology studies can be useful in assessing response to quinidine in Brugada Syndrome, currently, there is no definitive way to monitor drug effect in an individual. The QUIET BrS Study will investigate the effect of quinidine on a variety of clinical parameters in patients with Brugada syndrome. We seek to identify non-invasive markers of quinidine effect in patients with Brugada Syndrome which could be used to develop a non-invasive strategy for monitoring medical therapy in these patients and reduce the need for invasive procedures.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria1

  • Diagnosis of Brugada Syndrome

Exclusion Criteria6

  • Current treatment with drug known to prolong QT interval
  • Baseline QTc >450msec for men, > 460msec for women
  • Baseline QRS > 130msec
  • Baseline PR >200msec
  • Patients taking medications known to interact with quinidine
  • Known hypersensitivity to quinidine

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Interventions

Hydroquinidine 300mg, oral capsule, twice daily For 2 weeks Adherence will be monitored by patient report and tablet return. Serum quinidine levels will also be performed. This is a non-randomise

Hydroquinidine 300mg, oral capsule, twice daily For 2 weeks Adherence will be monitored by patient report and tablet return. Serum quinidine levels will also be performed. This is a non-randomised trial.


Locations(1)

Royal Prince Alfred Hospital - Camperdown

NSW, Australia

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