RecruitingACTRN12622000447752

Evaluating the effects of Vitamin K supplements on Aortic Stenosis

A randomised trial evaluating the effect of phylloquinone on the progression of mild to moderate aortic stenosis


Sponsor

University of Western Australia

Enrollment

108 participants

Start Date

Jul 1, 2023

Study Type

Interventional

Conditions

Summary

Calcific aortic stenosis is a condition in which build-up of calcium on the aortic valve, located at the outflow of the heart, progressively blocks blood flow to the organs and can cause debilitating symptoms and very poor survival. Timely replacement of the valve can be lifesaving but comes with significant risks and at high cost. The incidence is increasing in Australia. Until now there have been no treatments that can prevent the progressive obstruction of the aortic valve. Our pilot study showed that supplementation of Vitamin-K, 10mg per day is safe and can prevent all early types of calcification in the arteries. The double-blind, randomised, placebo-controlled PASSPORT trial will test whether Vitamin-K can slow or prevent the calcium build-up and obstruction of the aortic valve. 108 subjects with mild or moderate aortic stenosis on echocardiography will be randomised to Vitamin K1 10mg per day or matching placebo for a median duration of 16 months (range 12-21 months). All subjects will receive an echocardiogram and non-contrast CT-calcium score at baseline and at the end of the trial. The primary end point will be progression in aortic valve calcium score on CT scans and secondary outcomes will be progression of flow obstruction parameters as assessed by echocardiography.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria4

  • Aged 18+ years
  • Mild to moderate calcific aortic stenosis (peak flow velocity greater than 2.5m/s and less than 4m/s)
  • Valve area greater than 1 cm2
  • At least mild aortic valve calcification (Rosenhek category=1) on echocardiography.

Exclusion Criteria8

  • Planned procedure to unblock heart arteries
  • Clinically important disease of any heart valve
  • Kidney disease (eGFR<40ml/min)
  • Intolerance to Vitamin-K
  • Prescribed a Vitamin-K blocker or supplement
  • Heart rhythm disturbance preventing a good quality CT-calcium score scan
  • Pregnancy
  • Unlikely to complete the 12 months follow-up.

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Interventions

Vitamin-K1 10 mg oral capsules, daily for minimum 12 months (last in) and up to 21 months (first in) with median duration 16 months. Participants will receive their randomised treatments in 3-month

Vitamin-K1 10 mg oral capsules, daily for minimum 12 months (last in) and up to 21 months (first in) with median duration 16 months. Participants will receive their randomised treatments in 3-month allocations. Every 3 months existing treatments will be returned. Adherence will be assessed by pill counts and completion of the Morisky scale.


Locations(1)

Royal Perth Hospital - Perth

WA, Australia

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