Menu
Not yet recruiting NCT06671769

Natural Heart Health Supplement Trial

Phase I Interventional Cholesterol Cholesterol (total and HDL)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Heart Health Supplement.
Who it may be relevant to
Registry conditions: Cholesterol, Cholesterol (total and HDL). Basic parameters: from 21 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

We are running a 3-month trial of an experimental natural heart health supplement. Participants will take a daily dose of an experimental natural heart health supplement in powdered format, chocolate flavor. The trial will assess changes in heart biomarkers such as Total Cholesterol, HDL-C, LDL-C, Triglycerides, and High-Sensitivity C-reactive protein (hs-CRP).

Detailed description

Heart disease is a leading cause of death in the United States, and maintaining healthy cholesterol levels is crucial for heart health. While social media and the press have focused on trendier treatments for general longevity, for most of us keeping our cholesterol in check will make a major impact. Research indicates that natural substances long used in Eastern medicine, can positively affect cholesterol levels and reduce inflammation, both vital for cardiovascular wellness.

This study aims to empower participants with evidence-based insights about the effectiveness of a natural heart health supplement in managing cholesterol levels and reducing inflammation. By participating, you'll contribute to valuable research while potentially enhancing your heart health through natural means.

This study aims to assess the impact of a natural heart health supplement on Total Cholesterol, HDL-C, LDL-C, Triglycerides, and hs-CRP levels over three months. Our objective is to provide evidence supporting or refuting the supplement's efficacy.

Interventions

  • Dietary supplement Heart Health Supplement
    This is a natural heart health supplement in powdered format, chocolate flavor where participants will take a daily dose.

Primary outcome measures

  • Total Cholesterol [Time frame: from Baseline to 30 day and 90 day.]
  • HDL Cholesterol [Time frame: from baseline to 30 day and 90 day]
  • LDL Cholesterol [Time frame: Baseline to 30 day and 90 day]
  • Triglycerides [Time frame: From baseline to 30 day and 90 day]
Secondary outcome measures (1)
  • hs-CRP [Time frame: from baseline to 30 day and 90 day]

Eligibility criteria

Exclusion criteria

  • Individuals with known soy allergies
  • Individuals with liver disease
  • Pregnant or breastfeeding individuals

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • Efforia - Study will be entirely online — New York

Identifiers

NCT: NCT06671769 · 34661

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗