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Clinical effectiveness of Unani drugs in comparison to conventional drug in the treatment of dyslipidaemia (abnormal amount of fat in the blood)

A Randomized, Standard Controlled, Clinical Study to Evaluate the Safety and Efficacy of JawαÌ?rish Falafili in the Treatment of FartÌ£-e- Tadassum fiâ??l Dam (Dyslipidaemia) - PGDL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019066
Enrollment
60
Registered
2019-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: E789- Disorder of lipoprotein metabolism, unspecified

Interventions

Intervention1: Group A: Study Group (Unani Drug group): JawaÌ?rish falafili: Method of Preparation- The drug will be prepared in single batch on the guidelines and method of preparation described in

Sponsors

Central Research Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants of any sex aged 30-60 years. Participants with having following lipid or lipoprotein 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. Both obese and non-obese.

Exclusion criteria

Exclusion criteria: Participants aged less than 30 and more than 60 years. Participants having a co-morbid condition like IHD, HT, Diabetes, etc. Participants having a major systemic disorder which interferes in the present study. Pregnant or Lactating Women. Significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction Known cases of Immunocompromised states (HIV/ AIDS, etc.)/Malignancies Participant not willing to attend treatment schedule regularly

Design outcomes

Primary

MeasureTime frame
Biochemical assessment of the change in Lipid and Lipoprotein levelTimepoint: At baseline, 2nd, 3rd and 4th followups

Secondary

MeasureTime frame
Hemogram LFT, RFT, FPG, ECG and Urine R/M examinationTimepoint: At baseline, 3rd followup and after treatment, except ECG that will be at baseline and after treatment

Countries

India

Contacts

Public ContactQamar Uddin

Central Research Institute of Unani Medicine

ccrumnawab@gmail.com8100992044

Outcome results

None listed

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