Higher Cholesterol levels in blood.

A Randomised controlled trail to evaluate the efficacy of Ayurveda Intervention (Nitya Virechana)as an add-on to Standard Care in Secondary Hyperlipidemia. - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067265

Enrollment

Registered

2024-05-14

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Health Condition 1: E784- Other hyperlipidemia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of all genders between the age group of 20-65 years who fulfil the criteria of Objective and Subjective parameters. 2.Controlled HTN -less than or equal to 140/90 mm of Hg. 3.Controlled NIDDM -HbA1C less than or equal to 7%. 4.Patients fulfilling the diagnostic criteria of Hyperlipidaemia. 5.Patients already on Antilipidemic drugs since 0-10years. 6.Patients fit for Nitya Virechana.

Exclusion criteria

Exclusion criteria: 1.Patients newly diagnosed and not on Antilipidemic drugs. 2.Induced Hyperlipidaemia due to prolonged intake of Glucocortiosteriods. 3.Patients suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Tuberculosis, Psycho-Neuro-Endocrinal disorders, CKD, Nephrotic Syndrome, Liver disorders etc.) 4.Patients with a past history of Atrial Fibrillation, Acute Coronary Syndrome, 5.Patient with evidence of malignancy. 6.Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
Reduction in Cholesterol levelsTimepoint: 45days	—

Secondary

Measure	Time frame
Weight lossTimepoint: 45days	—

Countries

India

Contacts

Public ContactNandini RD

Ayurveda Mahavidhyalaya Hospital

padmavatikulkarni203@gmail.com9448235819

Outcome results