Ancient herb vs. modern vitamins: which boosts heart health?
NCT ID NCT07206901
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed trial tested an Ayurvedic herbal supplement called Maharishi Amrit Kalash (MAK) against vitamins C+E and a placebo in 143 Black adults aged 55+ with heart disease or high risk. The goal was to see if MAK improves blood vessel function, measured by how well arteries widen with increased blood flow. Results could suggest whether this herbal compound supports heart health better than vitamins or placebo.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Maharishi Amrit Kalash (Ayurvedic herbal supplement)
- What this could lead to
- If it works, this could point toward a natural supplement that improves blood vessel health in people at high risk for heart disease.
- What could go wrong
- This is a small, completed trial with no phase designation, so results may not be conclusive. The supplement is not a proven treatment and should not replace standard heart medications.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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143 people
The number who actually took part.
- Started
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Oct 2002
- Finished
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Oct 2014
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
55 to 90 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Ethnicity: African American, self-identified * Age: 55 years and older * Medically documented coronary artery disease (CAD/CHD): defined by previous myocardial infarction OR revascularization procedure-coronary artery bypass grafting (CABG), or percutaneous transluminal coronary angioplasty (PCTA), OR coronary angiography with at least one coronary artery with \> 50% stenosis. * In the absence of documented CAD/CHD above, then at least two risk factor points on the Framingham/ATPIII risk factor scoring assessment. * Signed informed consent * Permission of Participant's primary physician (if feasible) Exclusion Criteria: * Myocardial infarction, unstable angina, coronary artery by-pass grafting (CABG), percutaneous transluminal coronary angioplasty (PTCA), or stroke within preceding three months. * Carotid artery endarterectomy. * Arrhythmia atrial fibrillation, second or third degree AV block. * Congestive heart failure-Class III or IV or ejection fraction less than 30 percent. * Clinically significant valvular heart disease. * Clinically significant hepatic or renal failure. * Major psychiatric disorders, current alcohol/dependency disorder, or other drug abuse dependency disorder. * Non-cardiac life threatening illness. * Participating in a formal stress management program. * Plans to move out of the study area or travel extensively. * Unwillingness to accept randomization into any study group.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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College of Integrative Medicine
Fairfield, Iowa, 52556, United States
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