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A Prospective Trial of Ayurveda for Coronary Artery Disease

A Prospective Trial of Ayurveda for Coronary Artery Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02228343
Enrollment
22
Registered
2014-08-29
Start date
2013-01-31
Completion date
2014-01-31
Last updated
2024-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Brief summary

Can Ayurvedic therapy improve markers of cardiovascular health and cardiovascular risk factors in patients with coronary artery disease.

Detailed description

Patients with established coronary artery disease will be treated with 90 days of Ayurvedic therapy to include yoga, meditation, breathing exercises,and herbs. Arterial stiffness, weight, BMI, BP, medications, cholesterol, LDL, HDL, triglyceride, HS-CRP will be measured at baseline and after 90 days of therapy.

Interventions

Ayurveda includes meditation, yoga, breathing exercises, herbs

Sponsors

University of New Mexico
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* stable coronary artery disease (prior mi, coronary angioplasty or stent, coronary bypass surgery)

Exclusion criteria

* age \< 18 years * life expectancy \< 6 months * pregnancy or breast feeding * unwilling or unable to complete 90 days of therapy * already receiving/taking Ayurvedic therapy * unable to converse in or understand English language

Design outcomes

Primary

MeasureTime frame
Participants With Arterial Stiffness Were Measured as Pulse Wave Velocity Meters/Second3 months

Countries

United States

Participant flow

Participants by arm

ArmCount
Ayurveda
Ayurvedic therapy Ayurveda: Ayurveda includes meditation, yoga, breathing exercises, herbs
22
Total22

Baseline characteristics

CharacteristicAyurveda
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
22 Participants
Race and Ethnicity Not Collected— Participants
Region of Enrollment
United States
22 Participants
Sex: Female, Male
Female
NA Participants
Sex: Female, Male
Male
NA Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 19
other
Total, other adverse events
0 / 19
serious
Total, serious adverse events
0 / 19

Outcome results

Primary

Participants With Arterial Stiffness Were Measured as Pulse Wave Velocity Meters/Second

Time frame: 3 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
AyurvedaParticipants With Arterial Stiffness Were Measured as Pulse Wave Velocity Meters/Second19 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026