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Role of Haritaki Churna and Navak Guggulu in the treatment of high blood cholesterol levels

A study to determine the effect of Haritaki Churna and Navak Guggulu in the management of hyperlipidemia a randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059251
Enrollment
30
Registered
2023-10-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: E660- Obesity due to excess calories

Interventions

None listed

Sponsors

Amol Ganeshdas Khatri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age limit from 25 to 60 yrs. 2. Patient irrespective of age, sex, religion etc. of hyperlipidemia. 3. Obese and non-obese hyperlipidemic patients (BMI-18.50 to 40.00 kg/m2 as per New Updated WHO classification of BMI of 2004) 4. Patients with controlled Type 2 diabetes mellitus ( Fasting 5. Patients with high blood lipid profile. Lipid profile showing any one or more of the following criteria was considered diagnostic of hyperlipidemia a. Patient having Serum Total Cholesterol Level >200mg/dl. b. Patient having Serum Triglycerides Level > 150 mg/dl. c. Patient having Serum LDL Cholesterol Level >130mg/dl. d. Patient having serum VLDL Cholesterol Level > 40 mg/dl. e. Patient having Serum HDL Cholesterol Level < 40 mg/dl.

Exclusion criteria

Exclusion criteria: 1. Patients having a history of untreated thyroid disorder. 2. Pregnant women & lactating mother. 3. Chronic illness and infection like TB, CA and HIV infection. 4. Patient is suffering with psychological disorders like anxiety, depression. 5. Patient with Respiratory Diseases Complications, Coronary Heart Disease, Hepatic or Renal Disease etc. 6. Patients having drug induced hyperlipidemia like steroids.

Design outcomes

Primary

MeasureTime frame
Reduction in the values of Lipid Profile like Total Cholesterol, Serum Triglycerides, LDL, VLDL and increase in HDL levelsTimepoint: 60 days

Secondary

MeasureTime frame
Efficacy of drugs used in trial Timepoint: 30 & 60 days

Countries

India

Contacts

Public ContactDr Archana Dachehwar

Shri Ayurved Mahavidyalaya Nagpur

dr.dachewar@gmail.com9822206312

Outcome results

None listed

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