ClinicalTrials.gg
CompletedNCT05000541Updated Nov 7, 2023

Observation of the Effects of Guideline-driven Lifestyle Interventions, Including Use of a Red-yeast Based Nutraceutical

An observational study in Hypercholesterolemia, sponsored by Mylan Inc.. Completed at 7 sites in 2 countries. Open to participants aged 25 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-11-07.

Sponsored by Mylan Inc. (part of Viatris Inc.) · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
259
Ages
25 Years to 75 Years
Sex
All
01

Study summary

The objective of the present multinational, multicentre, prospective, scientific study is to confirm that prescription of a low-dose red yeast-based nutraceutical.

Read the detailed description

The objective of the present multinational, multicentre, prospective, scientific study is to confirm that prescription of a low-dose red yeast-based nutraceutical significantly increases the LDL-C lowering effect of guideline-driven lifestyle interventions in subjects with hypercholesterolemia at low-moderate cardiovascular risk not requiring a drug therapy.

02

Conditions studied

  • Hypercholesterolemia
03

In context

Hypercholesterolemia

1,175 studies on the registry are indexed under Hypercholesterolemia; 93 are open to participants now.

This study's enrollment of 259 is below the median of 1,000 across 144 observational studies indexed under Hypercholesterolemia.

Browse Hypercholesterolemia studies →

Lead sponsor

Mylan Inc. is the lead sponsor of 44 studies on the registry; none are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 9 (100%) have results posted.

First submitted after Mylan Inc. became part of Viatris Inc..

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Subjects to be enrolled are subjects already in primary prevention for CVD for raised LDL-C and who, according to the intervention strategies recommended in Table 5 of the ESC/EAS guidelines (lifestyle interventions, consider drug if uncontrolled) had been prescribed, in the previous 3 months, only dietary advices and physical exercise.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age between 25 and 75 years;
  • In primary prevention for low-moderate CV risk, with diet and physical exercise to control raised LDL-C level, for at least 3 months;
  • LDL-C > 100 mg/dL (2.6 mmol/L), \< 190 mg/dL (4.9 mmol/L)
  • CV risk SCORE \<5% (based on SCORE chart according to figure I for Poland respective figure 2 for Austria and Germany in the ESC/EAS guideline 2019);
  • Triglyceride \<400 mg/dL;
  • Advised to use nutraceutical as part of the lifestyle intervention as per guideline and within the product label (i.e. posology as in product label);
  • Written .

Exclusion criteria

Exclusion Criteria:

  • Subjects being treated or who have been treated for up to 3 months before the start of the study with lipid-lowering drugs or nutraceuticals including functional foods for which lipid-lowering effects are known (e.g. fish oil, sterol-containing yoghurts etc.);
  • Subjects involved in other clinical studies with pharmaceutical products
  • Known laboratory evidence of either liver, muscle, thyroid or kidney dysfunction;
  • Subjects with prior history of cardiovascular events or with high cardiovascular risk equivalents;
  • Uncontrolled hypertension (systolic blood pressure >190 mmHg or diastolic blood pressure >100 mmHg);
  • Pregnancy and breastfeeding.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
259 participants (actual)
Patient registry
No

Groups and cohorts

  • Armolipid-L/Armolipid Plus-L

    Armolipid-L used for participants in Germany and Poland Armolipid Plus-L used for participants in Austria

06

What researchers measure

Primary outcomes

  1. Mean change from baseline in LDL-C

    Mean change from baseline in LDL-C at 3 months

    Time frame: 3 months

Secondary outcomes

  1. Subjects' adherence to the prescribed lifestyle interventions measured on Visual Analogue Scale (VAS)

    Subjects' adherence (at 3 months and 6 months) to the prescribed lifestyle interventions measured on Visual Analogue Scale (VAS); minimum 0mm, maximum 100mm; higher value means better adherence

    Time frame: at 3 months and 6 months

07

Study locations

7 sites
  • Ordination
    Unterhautzenthal, 2011, Austria
  • Ordination
    Vienna, 1140, Austria
  • Medical Practice
    Bexbach, 66450, Germany
  • Medical Practice
    Deggingen, 73326, Germany
  • Medical Practice
    Frankfurt, 60598, Germany
  • Medical Practice
    Görlitz, 02827, Germany
  • AmBeNet GmbH
    Leipzig, 04107, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 7, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05000541
Lead sponsor
Mylan Inc.
Collaborators
Mylan Österreich GmbH, Mylan Germany GmbH, Mylan Healthcare Sp. z o.o.
Responsible party
Sponsor
First posted
Aug 11, 2021
Start date
Dec 8, 2020
Primary completion
Oct 31, 2023
Completion
Oct 31, 2023
Last update
Nov 7, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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