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A clinical trial to study the effects of Ayurvedic formulation Suved and Reimmugen (whole cow colostrum) in patients with atherosclerosis

A study to evaluate the results of integrative treatment (Ayurvedic capsules Suved and Reimmugen) for vascular disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN65795273
Enrollment
200
Registered
2016-11-07
Start date
2016-10-09
Completion date
Unknown
Last updated
2020-08-10

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

Conditions

Vascular disease, atherosclerosis Circulatory System

Interventions

Patients are randomised to one of two groups: 1. Suved (Ayurvedic formulation, FDA India approved) and whole cow colostrum Reimmugen. Dosage decided by regular Ayurvedic use Suved 500m

Sponsors

Health Solutions
Lead Sponsor
Smt. Kashibai Navale Medical College
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Males or females aged 18 or over with a diagnosis of vascular disease leading to IHD, CAD, CVD, DVT or PAD at any stage

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women 2. Patients below age of 18 3. Acute IPD operative condition 4. Patients undergoing interventional procedures/surgical treatments other than for vascular disease, until they are discharged from intensive care 5. Haemorrhagic cerebrovascular stroke

Design outcomes

Primary

MeasureTime frame
Restoration of carotid IMT to a non-pathological state, supported with positive changes in functionality and relief from associated symptoms: 1. Clinical investigations will be compared pre - post treatment to evaluate percent changes in IMT and cardiac function as a mark of reversal of atherosclerosis and relief from symptoms associated with blockages in blood vessels due to atherosclerosis. IMT measurements are taken as standard to evaluate atherosclerosis and 2D echo taken for cardiac perfusion. 2. Functional changes considered on the basis of symptoms of chest pain, breathlessness, stamina of walking or performing daily chores. Measured at baseline and at the end of 3 months of treatment.

Secondary

MeasureTime frame
Development of ischaemic events in other circulations (e.g., in a stroke patient, evaluation of coronaries), assessed at baseline and at the end of 3 months of treatment.

Countries

India

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026