Title:Efficacy and Safety of a Unani Pharmacopeial Powder Formulation and
Sharbat banafsha in Women with Uncomplicated Urinary Tract Infection:
A Pilot Self-Control Clinical Trial
Volume: 21
Issue: 4
Author(s): Arshiya Sultana*, Khaleequr Rahman and khadija Khaleeq
Affiliation:
- Department of Ilmul Qabalat wa Amraze Niswan (Gynecology and Obstetrics), National Institute of Unani Medicine, Ministry of Ayush, GOI, Bengaluru, India
Keywords:
Female diseases, health-related quality of life, UTISA questionnaire, uncomplicated urinary tract infection (UTI), Unani Medicine, clinical trial.
Abstract:
Background: Antimicrobial resistance is a growing global concern, highlighting the
urgent need for effective non-antibiotic alternatives to treat urinary tract infections. Effortlessly
blending traditional Unani knowledge with modern scientific evaluation, this study highlights
the potential of Unani formulations in managing uncomplicated UTIs. This study's findings underscore
the importance of exploring and bridging the gap between Unani medicine and evidence-based practices. This study investigates the efficacy and safety of an Unani Pharmacopeial
powder formulation and Sharbat Banafsha in treating women with uncomplicated urinary
tract infections (UTI).
Materials and Methods: The pre and post-test pilot self-control clinical study involved 13 participants
with uUTI who received 3.5 g powder Unani formulation comprising Lagenaria
siceraria (Molina) Standl, Malva sylvestris L., Cucumis sativus L. and Cucumis melo L., Portulaca
oleracea L., and Adiantum capillus L. with Sharbat Banafsha (syrup of Viola odorata L.)
25 ml twice daily for 8 days. The primary outcomes were assessed using the urinary tract infection
symptoms assessment (UTISA) questionnaire, while secondary outcomes included urine
culture and sensitivity, as well as health-related quality of life (HRQoL) assessment using the
SF-12 health survey. The data was analyzed, and p<0.05 was considered significant.
Results: The UTISA total score from 15.69 ± 2.18 was reduced to 4.00 ± 5.07 on day 9 with a
significance difference (p < 0.001). On day 14, 84.61% of the population had negative cultures.
The total SF-12, PCS, and MCS scores showed significant differences from Day 0 to 60
(p>0.05). No adverse effects were reported in both groups. HPLC analysis confirmed the presence
of the plant metabolite luteolin in both the powder and syrup.
Conclusion: The data explores the effectiveness of Unani formulations for bacterial urinary
tract infections (UTI), showing no adverse effects while also improving the HRQoL of women.
These herbal products contain luteolin, a bioactive molecule with antimicrobial properties.
Clinical Trial Registration Number: CTRI/2020/02/023404 dated 17/02/2020.