| Article Access Statistics|
| Viewed||2266 |
| Printed||56 |
| Emailed||0 |
| PDF Downloaded||142 |
| Comments ||[Add] |
Click on image for details.
| RESEARCH ARTICLE
|Year : 2015 | Volume
| Issue : 1 | Page : 72-79
Safety and efficacy of Qurse-e-istisqua in chronic hepatitis C Infection: An exploratory study
Harmeet Singh Rehan1, Deepti Chopra2, Madhur Yadav3, Neeta Wardhan4, Seema Manak1, KM Siddiqui5, Mohd Aslam6
1 Department of Pharmacology, Lady Hardinge Medical College, New Delhi, India
2 Department of Pharmacology, HIMSR, Jamia Hamdard, New Delhi, India
3 Department of Medicine, Lady Hardinge Medical College, New Delhi, India
4 Department of Pharmacology, University College of Medical Sciences, New Delhi, India
5 Central Council for Research in Unani Medicines, AYUSH, Ministry of Health and Family Welfare, Janak Puri, New Delhi, India
6 Department Pharmacology Ilmul Advia, faculty of Unani Medicine, Hamdard University, New Delhi, India
Background: Qurse-e-istisqua (Q-e-I), an Unani medicine commonly prescribed to treat liver disorders.
Objectives: To study efficacy and safety of Q-e-I in hepatitis C virus (HCV) infection.
Methods : In this randomized double-blind exploratory study, 60 naive patients of HCV infection were assigned to receive either interferonα2a (IFNα2a) (3 mIU, subcutaneous, thrice weekly), ribavirin (RBV) (1000 mg, orally, twice daily in divided doses) and placebo (n = 30) or IFNα2a, RBV and Q-e-I (5 g, orally, thrice daily in divided doses) (n = 30). HCV RNA levels, serum hyaluronic acid (SHA), ultrasound image scoring for fibrosis, liver and renal function test, prothrombin time, were done at the baseline and thereafter periodically.
Results: Early virologic response (EVR), end of treatment response (ETR) and sustained virologic response (SVR) were 90%, 96.6% and 90% in the control group and 86.6%, 90.0% and 83.3% in the treatment group. SHA level was lower in the treatment group at the end of the treatment as compared to the control group. Mean end of follow-up ultrasound image scoring for fibrosis in the control and the treatment group was 1.37 ± 0.07 and 1.22 ± 0.06 respectively. Aspartate aminotransferase (AST) levels were significantly lower in the treatment group than the control group at 1-month. Commonly observed adverse drug reactions included fever, hair fall, fatigue, anemia, and diarrhea.
Conclusion: Q-e-I was well tolerated and showed anti-fibrotic activity. EVR, ETR and SVR suggested that Q-e-I do not have any anti-HCV activity. Early recovery in AST and inhibition of progress of fibrosis in Q-e-I group was probably due to the anti-inflammatory and antioxidant activity of its ingredients.
Dr. Harmeet Singh Rehan
Department of Pharmacology, Lady Hardinge Medical College, New Delhi
Source of Support: None, Conflict of Interest: None
[FULL TEXT] [PDF]*