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Efficacy of a Unani formulation in Dyslipidaemia

A Prospective, Randomized, Parallel Group, Open Label, Active Controlled Clinical Study to Evaluate the Efficacy and Safety of Unani Formulation in the Management of Fart-i-Tadassum Fi’l Dam (Dyslipidaemia) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059299
Enrollment
60
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: E00-E89- Endocrine, nutritional and metabolic diseases

Interventions

Intervention1: Study Group (Unani Drug group): Qurs-e-Zarishk: Method of Preparation- The drug will be prepared in single batch on the guidelines and method of preparation described in the National Fo

Sponsors

National Research Institute of Unani Medicine For Skin Disorders
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Newly diagnosed participants of any sex aged 30-60 years. Participants having any one or more of following lipid abnormality in blood: Serum Cholesterol equal to or more than 200mg/dl. HDL-C less than 40 mg/dl. LDL Cholesterol equal to or more than 130 mg/dl. Serum Triglycerides level equal to or more than 150mg/dl and/or less than 400 mg/dl. Body Mass Index (BMI) 23-40 kg/m2.

Exclusion criteria

Exclusion criteria: Participants having hypothyroidism, diabetes mellitus, history and clinical evidence of angina, myocardial infarction (MI). Pregnant or Lactating Women. Significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction. Known cases of Immunocompromised states (HIV/ AIDS, etc)/ Malignancies. Participants not willing to attend treatment schedule regularly.

Design outcomes

Primary

MeasureTime frame
Change in serum triglyceride level from baseline to post treatment(8weeks).Timepoint: At baseline, 4th weeks and 8 weeks.

Secondary

MeasureTime frame
Change in total cholesterol (TC), low density lipoprotein (LDL), and increase in high density lipoprotein (HDL). Change in BMI, Weight, Waist, Hip, and Waist/Hip ratio from baseline to post treatment at 8weeks.Timepoint: At baseline, 4th weeks and 8th weeks.

Countries

India

Contacts

Public ContactDr.Hafsa Patel

National Research Institute of Unani Medicine For Skin Disorders

ccrumnawab@gmail.com8100992044

Outcome results

None listed

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