Actively Recruiting

Phase Not Applicable
Age: 30Years - 70Years
All Genders
NCT07429227

Evaluation Through Innovative Examinations of Intestinal Dysbiosis Status in Patients Diagnosed With Cardiovascular Diseases and Evaluation of the Efficacy of Natural and Probiotic Extracts in the Non-pharmacological Approach to Improving Intestinal Dysbiosis Status.

Led by Casa di Cura Dott. Pederzoli · Updated on 2026-02-24

15

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

C

Casa di Cura Dott. Pederzoli

Lead Sponsor

H

Herboplanet Srl

Collaborating Sponsor

AI-Summary

What this Trial Is About

The prospective experimental study aims to take an instantaneous photograph of the subject at time T0 and after 24 hours of intestinal permeability and dysbiosis indices in patients with acute coronary syndromes (ACS) which include unstable coronary artery disease (unstable angina) and acute myocardial infarction (AMI). The aim is to verify whether essential oils in particular formulations with high bioavailability are able to re-establish intestinal eubiosis after 2 months, confirmed by tests laboratory specifics such as metabolomics.

CONDITIONS

Official Title

Evaluation Through Innovative Examinations of Intestinal Dysbiosis Status in Patients Diagnosed With Cardiovascular Diseases and Evaluation of the Efficacy of Natural and Probiotic Extracts in the Non-pharmacological Approach to Improving Intestinal Dysbiosis Status.

Who Can Participate

Age: 30Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signing of informed consent
  • Diagnosis of Acute Coronary Syndrome (ACS)
  • Age between 30 and 70 years
Not Eligible

You will not qualify if you...

  • Use of lipid-lowering drugs (statins, ezetimibe, fibrates) within 3 months before consent
  • Use of lipid-lowering nutraceuticals containing monacolin K within 3 months before consent
  • Use of monoclonal antibodies inhibiting PCSK9 (e.g., Evolocumab, Alirocumab) within 3 months before consent
  • Diagnosis of HIV, cancer, or diabetes type I or II
  • Female patients who become pregnant during the trial will be withdrawn

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ospedale P. Pederzoli Casa di Cura Privata S.p.A.

Peschiera del Garda, Verona, Italy, 37019

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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