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NCT Number: NCT05861648

Folic Acid Supplementation in Calcific Aortic Valve Disease

This is a prospective, randomized, comparative, clinical trial conducted by Wuhan Union Hospital that aims to evaluate the efficacy and safety of folic acid compared to placebo in patients with calcific aortic valve disease with mild aortic valve stenosis.

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Key information

About this study

Folic acid is involved in important physiological activities in the body such as DNA synthesis, cell division and growth and development. Recent studies have shown that folic acid may also have a positive effect on cardiovascular system health. Aortic valve calcification is a cardiovascular disease whose incidence increases progressively with age. Early studies suggest that folic acid may slow the progression of aortic valve calcification by inhibiting cell calcification and promoting calcium deposition. Participants were randomized into two groups: one group was given oral folic acid treatment and the other group was given placebo control. Patients in both groups were observed for aortic valve calcification during the follow-up period, and changes in aortic valve thickness, degree of calcification, and flow were recorded by cardiac ultrasonography, while the incidence of cardiovascular events and adverse effects were assessed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female adult ≥ 35 years of age at the time of recruiting.
  • Subject has calcific aortic valve disease with mild to moderate aortic valve stenosis as defined by Doppler echocardiography results: Aortic Valve mean pressure gradient between 10-30 mmHg and Aortic Valve Area ≥ 1.2 and ≤ 2.0 cm2 on transthoracic echocardiography within 2 weeks prior to randomization and Cardiac Compute Tomography (CT) test results: aortic valve calcium score (Agatston score) ≥ 200 AU at baseline cardiac CT within 1 month prior to randomization
  • Subject provides written informed consent prior to initiation of any study procedures.
  • Subject understands and agrees to comply with planned study procedures.

Exclusion criteria

  • Subject has concomitant moderate or severe mitral or tricuspid valve disease.
  • Subject has left ventricular ejection fraction < 50%.
  • Subject previous history of aortic valve surgery, pancreatitis, malignant tumor, drug or alcohol abuse.
  • Subjects whose alanine aminotransferase (ALT) and aspartate aminotransferase (AST) > 2.5 times the upper limit of normal range.
  • Subjects who cannot undergo Cardiac CT.
  • Pregnant or lactating women.
  • Consideration by the investigator, for safety reasons, that the subject is an unsuitable candidate to receive study treatment.

Treatment and study plan

Folic Acid Oral Tablet

Drug

Dietary Supplement: Folic acid 2.5mg/day

Placebo

Dietary Supplement

Dietary Supplement: Placebo

Primary outcomes

  1. Aortic valve calcification

    Time frame: 104 weeks

    Aortic valve calcification as measured by change from baseline in Agatston arbitrary unit (AU) using cardiac computed tomography (CT) at 104 weeks

  2. overall survival

    Time frame: 3 years

    overall survival (OS)

Secondary outcomes

  1. Time-to-major adverse cardiovascular events

    Time frame: 104 weeks

    Time-to-major adverse cardiovascular events of cardiac death, non- fatal myocardial infarction, heart failure hospitalization and stroke

  2. Aortic valve calcification

    Time frame: at week 52

    Change in aortic valve calcification as measured by Agatston AU using cardiac computed tomography (CT) at week 52

  3. Change in aortic valve stenosis severity

    Time frame: at week 104

    Change in aortic valve stenosis severity as measured by peak transaortic velocity using echocardiography at week 104 as compared to baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Fei Li, MD

CONTACT

[email protected]

15972969897 ext. +86

Li Xu, MD

CONTACT

[email protected]

15387030212 ext. +86

Sponsors and collaborators

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Other

Registry information

Official study title

Effect of Folic Acid Supplementation in Patient's Calcific Aortic Valve Disease With Mild Aortic Valve Stenosis

Important dates

Study start
2023
Primary completion
2025
Study completion
2028
First posted
May 17, 2023
Registry last updated
May 17, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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