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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03243890
Other study ID # AVADEC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 12, 2018
Est. completion date May 1, 2021

Study information

Verified date September 2022
Source Odense University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aortic stenosis is a common heart valve disease and due to the growing elderly population the prevalence is increasing. The disease is progressive with increasing calcification of the valve cusps. A few attempts with medical preventive treatment have failed, thus presently the only effective treatment of aortic stenosis is surgery. This study will examine the effect of menaquinone-7 (MK-7) supplementation on progression of aortic valve calcification (AVC). The investigators hypothesize that MK-7 supplementation will slow down the calcification process.


Recruitment information / eligibility

Status Completed
Enrollment 389
Est. completion date May 1, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers No
Gender Male
Age group 65 Years to 75 Years
Eligibility Inclusion Criteria: Participants in the Danish Cardiovascular Screening Trial (Trials. 2015 Dec 5;16:554) with an aortic valve calcification score above 300, but without aortic valve stenosis are eligible. Exclusion Criteria: - Known aortic valve disease (peak velocity =3.0 m/s) - History of venous thrombosis or other coagulation disorders or use of vitamin K antagonists - Disorders of calcium and phosphate metabolism - A life-expectancy < 5 years

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Menaquinone-7 720 µg/day including the recommended daily dose of vitamin D (25 µg/day).
Half of the patients are randomized to supplementation with MK-7 (720 µg/day) including the recommended daily dose of vitamin D (25 µg/day).
Placebo
Half of the patients are randomized to placebo treatment (no active treatment).

Locations

Country Name City State
Denmark Department of Cardiology, Odense University Hospital Odense Odense C

Sponsors (1)

Lead Sponsor Collaborator
Axel Diederichsen

Country where clinical trial is conducted

Denmark, 

References & Publications (1)

Lindholt JS, Frandsen NE, Fredgart MH, Øvrehus KA, Dahl JS, Møller JE, Folkestad L, Urbonaviciene G, Becker SW, Lambrechtsen J, Auscher S, Hosbond S, Alan DH, Rasmussen LM, Gerke O, Mickley H, Diederichsen A. Effects of menaquinone-7 supplementation in patients with aortic valve calcification: study protocol for a randomised controlled trial. BMJ Open. 2018 Aug 23;8(8):e022019. doi: 10.1136/bmjopen-2018-022019. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Aortic valve calcification The primary endpoint is the change in aortic valve calcification. The natural history of the aortic valve calcification is not adequately understood, and accordingly the changes are analyzed in two prespecified patient subgroups (AVC score 300-599 and =600, respectively). From baseline to two years of follow-up
Secondary Arterial calcification Change in compiled arterial calcification by non-contrast CT From baseline to two years of follow-up
Secondary Aortic size Change in aortic diameter From baseline to two years of follow-up
Secondary Coronary plaque composition Change in total plaque burden in the coronaries and carotid arteries by contrast CT From baseline to two years of follow-up
Secondary Aortic valve area Change in aortic valve area by transthoracic echocardiography From baseline to two years of follow-up
Secondary Bone mineral density Change in bone mineral density as quantitative CT of the columna lumbalis and hip region From baseline to two years of follow-up
Secondary Biomarkers of calcification Change in matrix-Gla proteins and osteocalcin with different phosphorylation (p and dp) and carboxylation forms (c and uc). From baseline to two years of follow-up
Secondary Quality of life Change in quality of life From baseline to two years of follow-up
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