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Study identifier: NCT04186286 Synced from ClinicalTrials.gov · July 28, 2026
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Crossover Study of Propranolol vs Ivabradine in POTS

Condition: Postural Tachycardia Syndrome  ·  Sponsor: University of Calgary

PhasePhase 2
Planned participants20
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

1.0 BACKGROUND Postural tachycardia syndrome (POTS) is a disorder of chronic orthostatic intolerance characterized by symptoms of palpitations, lightheadedness, chest discomfort, shortness of breath, blurred vision, and mental clouding. These symptoms occur during standing and are associated with a marked increase in heart rate (HR) in the absence of hypotension, which typically resolve when sitting or lying down. Most importantly, POTS is associated with a very poor quality of life and significant functional disability. POTS patients commonly experience mental clouding ("brain fog") even while lying down or seated, which poses significant limitations to daily activities . Unfortunately, there is a relative paucity in the literature assessing therapies for POTS patients. Given that excessive tachycardia on standing is a fundamental component of this syndrome, a handful of studies have evaluated medications that reduce HR. Ivabradine is newer drug that is a selective If channel blocker that reduces HR without affecting other cardiovascular functions. 2.0 RATIONALE / STUDY PURPOSE The investigators propose to compare the efficacy of propranolol and ivabradine on HR response to standing, and symptom burden in patients with POTS. 3.0 Study Design This will be a single-center double-blind placebo-controlled randomized crossover trial conducted in patients with POTS to compare effects of (1) oral ivabradine 5 mg bid plus placebo BID (to fill out a QID schedule); (2) oral propran…

This description comes directly from the study's public registry record.

Talk to the study team

Satish Raj, MD  ·  403-210-6152  ·  autonomic.research@ucalgary.ca

Shahana Safdar  ·  403-220-8897  ·  ssafdar@ucalgary.ca

Always discuss trial participation with your own doctor first.

Locations (1)

University of CalgaryCalgary, Alberta, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT04186286