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Clinical efficacy of Gojihvadi Kwath, Shirishadi Kwath, Sanjeevani Vati, Panchagavya Ghrita Granules & Shunthi Churna for COVID-19 management, a randomized controlled trial

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Title Clinical efficacy of Gojihvadi Kwath, Shirishadi Kwath, Sanjeevani Vati, Panchagavya Ghrita Granules & Shunthi Churna for COVID-19 management, a randomized controlled trial
 
Creator Byadgi, Parameswarappa S
Kumari, Meena
Singh, Vishwambhar
Dwivedi, Arun Kumar
Mishra, Sunil Kumar
Dubey, Sushil Kumar
Chaudhary, Ashvanee Kumar
Chaurasia, R N
Joshi, Namrata
Jani, Hitesh
Mishra, Rajeev Kumar
Singh, T B
P S, Arunima
Jayakumar, Remya
 
Subject Ayurveda
COVID-19
Gojihvadi Kwath
Panchagavya Ghrit Granules
Shirishadi Kwath
Sanjeevani Vati
 
Description 729-738
The obscure disease pattern of COVID -19 have to be evaluated with Ayurvedic interventions and the present clinical trial was a randomized open label parallel three-arm control trial on the major and minor symptomatic patients with the recent pandemic. The patients were recruited from the Super specialty building of Sir Sunderlal hospital, COVID- 19 ward and home isolated ones. The Ayurvedic intervention includes the 15 days oral administration (Group A) –Gojihvadi Kwath, Sanjeevani Vati; Panchagavya Ghrit Granules; Shunthi (Dry ginger powder) plus conventional treatment, in (Group B) –Shirishadi Kwath, Sanjeevani Vati; Panchagavya Ghrit Granules; Shunthi (Dry ginger powder) plus conventional treatment and in Group C (control group) only the conventional medicines. Assessment was done based on the RT-PCR reports, signs and symptoms. The results point out the efficacy of trial medicine (that is group A and B) to discharge the patients earlier than those from the control group. The early reduction in the signs and symptoms noted were also observed. Group B showed a faster recovery from dry cough and shortness of breath and improvement in appetite. Home-isolation patients showed faster recovery of clinical symptoms than the hospitalized patients. Ayurvedic interventions can accelerate viral load clearance associated with quicker recovery and concurrently decrease the risk of viral dissemination. Additionally, there were no adverse reactions observed with these trial medicines.
 
Date 2024-08-22T07:04:19Z
2024-08-22T07:04:19Z
2024-08
 
Type Article
 
Identifier 0975-1068 (Online); 0972-5938 (Print)
http://nopr.niscpr.res.in/handle/123456789/64438
https://doi.org/10.56042/ijtk.v23i8.13109
 
Language en
 
Relation Int Cl.24: A61K 9/00, A61K 36/00
 
Publisher NIScPR-CSIR,India
 
Source IJTK Vol.23(8) [August 2024]