Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06695429

Supplementation With Beetroot Juice to Prevent Contrast Associated Nephropathy During Hospitalization for Acute Coronary Syndrome Without ST Elevation

Led by Hospital General Universitario Santa Lucia · Updated on 2025-05-18

130

Participants Needed

1

Research Sites

155 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to compare the possible beneficial effect of beetroot juice supplementation versus the usual management during hospitalization to prevent contrast-induced nephropathy after cardiac catheterizations. The study includes patients diagnosed with non-ST elevation acute coronary syndrome with a possible indication for catheterism and high risk of kidney injury related to iodinated contrast. The intervention group will drink 500 mL (2 glasses daily, at breakfast and dinner) of beetroot juice added to the usual diet for 7 days or until hospital discharge and will receive the recommendation to maintain a diet rich in inorganic nitrates. The control group will receive the usual diet and recommendations. In both cases, other therapies will be prescribed to prevent contrast-induced nephropathy (hydration and statins) if there is no contraindication. Our hypothesis is that a compound present in beetroot juice, inorganic nitrates, can prevent the deterioration of kidney function related to contrast due to its vasodilatory effect, in addition to improving the subsequent prognosis of coronary heart disease due to its anti-inflammatory and antiproliferative effects, protector of the endothelium and inhibitor of platelet aggregation. Beetroot juice could also be beneficial in this context due to the antioxidant effect of the betalains it contains.

CONDITIONS

Official Title

Supplementation With Beetroot Juice to Prevent Contrast Associated Nephropathy During Hospitalization for Acute Coronary Syndrome Without ST Elevation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of acute coronary syndrome without persistent ST segment elevation with recommended invasive management
  • Moderate or high risk of contrast-induced nephropathy (Mehran score 16, excluding contrast volume)
Not Eligible

You will not qualify if you...

  • Under 18 years old or unable to give consent
  • Refusal to participate in the study
  • Known allergy to beetroot or its components
  • Pregnant
  • Unable to eat or drink orally
  • Serious illnesses limiting life expectancy to less than 1 year
  • On dialysis or predialysis at inclusion
  • Acute coronary syndrome with persistent ST elevation before inclusion
  • Shock or dependence on inotropic drugs at inclusion
  • Percutaneous coronary intervention already performed before inclusion
  • Receiving intravenous nitroglycerin for more than 1 hour before inclusion

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospital Universitario Santa Lucía

Cartagena, Spain

Actively Recruiting

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Research Team

J

Jose Manuel Andreu Cayuelas, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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