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NCT07487714Possibly a fitEnrolling by invitation

Comparing amiodarone doses for paroxysmal AF

Paroxysmal AFTreatment DecisionsTherapeutic Drug Monitoring (TDM)

Part of Heart & circulation clinical trials.

This study compares three different daily doses of the heart rhythm medication amiodarone to find the most effective one for preventing episodes of paroxysmal atrial fibrillation. Participants will take one of three doses (100, 200, or 400 mg) for up to 12 months, and the study will monitor how well each dose controls the irregular heartbeat.

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

Phase
Phase 4
Enrollment
80 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You must be over 18 years old.
  • You need to have a confirmed diagnosis of paroxysmal atrial fibrillation (a type of irregular heartbeat that comes and goes).
  • Your doctor must consider amiodarone a good treatment option for you.
  • You cannot have certain other heart conditions, such as severe coronary artery disease needing urgent treatment, or blood clots in the heart.
  • You must not be taking specific other medications (like some antidepressants, antibiotics, or heart rhythm drugs).
  • You cannot be pregnant or planning to become pregnant during the study.

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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