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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02917525
Other study ID # METC152045
Secondary ID
Status Recruiting
Phase Phase 2
First received September 26, 2016
Last updated March 21, 2018
Start date August 2016
Est. completion date December 2019

Study information

Verified date March 2018
Source Maastricht University Medical Center
Contact Bas Kietselaer, M.D., PhD
Phone +31 (0)43 687 5096
Email b.kietselaer@mumc.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Early development of calcified aortic valve disease (CAVD) is a commonly occurring complication in patients with a bicuspid aortic valve (BAV, an aortic valve consisting of two leaflets instead of three). In general, CAVD is characterized by progressive narrowing of the aortic valve, with involvement of altered calcium metabolism. CAVD progression in fact may lead to necessity of valve replacement, since to date, no other therapies have been shown effective in the treatment of CAVD.

The primary objective of our study is to test the hypothesis that supplementation of vitamin K2 will slow down the calcium metabolism in CAVD. Vitamin K2 is essential in the activation of matrix Gla Protein (MGP), an important inhibitory factor in the regulation of calcification.

In this randomized controlled trial, 44 patients will be allocated to either the vitamin K2 or placebo group. To assess the calcification process in a detailed manner in these patients, a Positron Emission Tomography (PET) scanner using a tracer (18F-fluoride [NaF]) that has been shown to bind to regions of newly developing microcalcification in aortic valve tissue is used.

We expect that vitamin K2 supplementation will reduce the calcium metabolism in the aortic valve on 18NaF-PET (primary endpoint) and slow progression of CAVD as measured by the calcium score on CT and echocardiography after 18 months (secondary endpoints), when compared to placebo.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- known bicuspid aortic valve

- calcified mild to moderate aortic valve stenosis on prior echocardiography

- informed consent provided

Exclusion Criteria:

- absence of calcified aortic valve stenosis on echocardiography

- presence of severe aortic valve stenosis

- history of aortic valve repair or replacement

- accepted atrial fibrillation

- use of oral anticoagulants

- claustrophobia

- presence of a pacemaker, ICD or ferromagnetic materials in the body

- life expectancy <2 years

- Pregnancy (current or wish for near future)

- soy allergy

- use of vitamin K-containing supplements

Study Design


Intervention

Dietary Supplement:
Vitamin K2

Other:
Placebo


Locations

Country Name City State
Netherlands Maastricht UMC Maastricht

Sponsors (1)

Lead Sponsor Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in aortic valve calcium metabolism Change in calcium metabolism, measured as uptake of the 18F-NaF tracer on a 18F-NaF PET/CMR scan Measured at baseline and 6 months
Secondary Change in aortic valve calcium score Change in aortic valve calcium score, measured on CT. Measured at baseline, 6 and 18 months
Secondary Progression of aortic valve stenosis Change of severity of aortic valve stenosis on echocardiography Measured at baseline, 6, 12 and 18 months
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