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NOT YET RECRUITING
NCT07881302
PHASE2

Effect of Ivabradine on Adolescent Dysautonomia

Sponsor: Kathryn Armstrong

View on ClinicalTrials.gov

Summary

Dysautonomia of Adolescence (dysautonomia) is an umbrella term used to describe symptoms experienced by adolescents and young adults related to dysfunction of the autonomic nervous system. Symptoms can include dizziness, fatigue, increased heart rate upon standing, exercise intolerance, and difficulty with daily activities. Treatment commonly involves lifestyle modifications, including increased fluid and salt intake and structured routines related to diet, sleep, aerobic exercise, and lower-body strength training. While these approaches can be effective, some patients experience symptoms that make it difficult to implement these changes. Despite increasing awareness of dysautonomia, research evaluating effective treatment strategies in adolescents remains limited, and there are currently no medications approved by Health Canada specifically for the treatment of dysautonomia. Ivabradine is a heart rate-lowering medication approved for the treatment of heart failure and has been studied as a potential treatment for symptoms associated with dysautonomia, including postural orthostatic tachycardia syndrome (POTS). However, there is limited evidence regarding its use in adolescents. The purpose of this randomized, double-blind, placebo-controlled study is to evaluate whether ivabradine can reduce symptom burden and improve heart rate control and overall well-being in adolescents with dysautonomia. The study will use a series of N-of-1 randomized controlled trials in which participants receive both ivabradine and placebo during different treatment periods. This design will allow the effects of ivabradine and placebo to be compared within individual participants.

Official title: A Series of N-of-1 Randomized Controlled Trials of Ivabradine for Improving Symptom Management in Adolescent Patients With Dysautonomia.

Key Details

Gender

All

Age Range

13 Years - 18 Years

Study Type

INTERVENTIONAL

Enrollment

5

Start Date

2026-11

Completion Date

2028-05

Last Updated

2026-10-19

Healthy Volunteers

No

Interventions

DRUG

Ivabradine

Participants will initially receive 2.5 mg of ivabradine orally twice daily with food. After 14 days of treatment, dosing will be reassessed. If there is insufficient symptom improvement, the Study Physician/Principal Investigator may increase the dose to 5 mg twice daily. Ivabradine will be prepared in 2.5 mg opaque capsules to maintain blinding.

DRUG

Placebo

Participants will receive matching placebo capsules orally twice daily with food. Placebo dosing will follow the same schedule as the ivabradine intervention, including a corresponding dose increase when required to maintain blinding. Placebo will be prepared in opaque capsules matching the ivabradine capsules.

Locations (1)

BC Children's Hospital

Vancouver, British Columbia, Canada