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Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba)
The disease Amlapitta has been selected for the clinical trials because it presents two type of manifestations depending upon the involvement of Agni (Ushnagunadhikya) and Jala (Dravagunadhikya) Mahabhuta. The present research work was focused at Drava Guna, with an aim to assess the efficacy of a d...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361927/ https://www.ncbi.nlm.nih.gov/pubmed/22661846 http://dx.doi.org/10.4103/0974-8520.96125 |
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author | Pol, Hemant More, Sharda Vyas, Mahesh Kumar Vyas, Hitesh Ravishankar, B. |
author_facet | Pol, Hemant More, Sharda Vyas, Mahesh Kumar Vyas, Hitesh Ravishankar, B. |
author_sort | Pol, Hemant |
collection | PubMed |
description | The disease Amlapitta has been selected for the clinical trials because it presents two type of manifestations depending upon the involvement of Agni (Ushnagunadhikya) and Jala (Dravagunadhikya) Mahabhuta. The present research work was focused at Drava Guna, with an aim to assess the efficacy of a drug with quality of Ruksha and Ushna predominance like Bhringaraja in treating Amlapitta with Pitta Drava Guna Vriddhi. Randomized open clinical trials were conducted on 22 patients of Amlapitta who were screened on the basis of clinical findings and allocated in to two groups. The criteria for selection were the signs and symptoms of Dravagunadhikya Amlapitta, irrespective of sex, religion, etc. Group A consisting of 15 cases received the trial drug Bhringaraja tablet (4 Tab. two times, 1 tablet=500 mg) and 7 cases in Group B received rice powder tablet as a placebo (4 Tab. two times, 1 tablet=500 mg) for 4 weeks. Special scoring pattern was adopted for the assessment of Amlapitta. Routine pathological tests such as blood, urine, stool, etc. were also carried out. In Group A, 55.33% patients showed marked improvement, whereas moderate improvement was observed in 26.67% patients. Complete cure was found in 06.67% of the patients and mild improvement in the chief complaints was observed in 13.33% patients. All the selected symptoms showed statistically significant results (P<0.01) except the Vidbheda in treated Group A, while in Group B, all symptoms showed statistically insignificant results except the Utklesha and Amlodgara. Total effect of the therapy showed statistically significant effect of the test drug. These results support the hypothesis |
format | Online Article Text |
id | pubmed-3361927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33619272012-06-01 Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) Pol, Hemant More, Sharda Vyas, Mahesh Kumar Vyas, Hitesh Ravishankar, B. Ayu Clinical Research The disease Amlapitta has been selected for the clinical trials because it presents two type of manifestations depending upon the involvement of Agni (Ushnagunadhikya) and Jala (Dravagunadhikya) Mahabhuta. The present research work was focused at Drava Guna, with an aim to assess the efficacy of a drug with quality of Ruksha and Ushna predominance like Bhringaraja in treating Amlapitta with Pitta Drava Guna Vriddhi. Randomized open clinical trials were conducted on 22 patients of Amlapitta who were screened on the basis of clinical findings and allocated in to two groups. The criteria for selection were the signs and symptoms of Dravagunadhikya Amlapitta, irrespective of sex, religion, etc. Group A consisting of 15 cases received the trial drug Bhringaraja tablet (4 Tab. two times, 1 tablet=500 mg) and 7 cases in Group B received rice powder tablet as a placebo (4 Tab. two times, 1 tablet=500 mg) for 4 weeks. Special scoring pattern was adopted for the assessment of Amlapitta. Routine pathological tests such as blood, urine, stool, etc. were also carried out. In Group A, 55.33% patients showed marked improvement, whereas moderate improvement was observed in 26.67% patients. Complete cure was found in 06.67% of the patients and mild improvement in the chief complaints was observed in 13.33% patients. All the selected symptoms showed statistically significant results (P<0.01) except the Vidbheda in treated Group A, while in Group B, all symptoms showed statistically insignificant results except the Utklesha and Amlodgara. Total effect of the therapy showed statistically significant effect of the test drug. These results support the hypothesis Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3361927/ /pubmed/22661846 http://dx.doi.org/10.4103/0974-8520.96125 Text en Copyright: © AYU (An International Quarterly Journal of Research in Ayurveda) http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Pol, Hemant More, Sharda Vyas, Mahesh Kumar Vyas, Hitesh Ravishankar, B. Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title | Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title_full | Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title_fullStr | Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title_full_unstemmed | Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title_short | Fundamental approach in the management of Drava Bahula Amlapitta with Bhringaraja (Eclipta alba) |
title_sort | fundamental approach in the management of drava bahula amlapitta with bhringaraja (eclipta alba) |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361927/ https://www.ncbi.nlm.nih.gov/pubmed/22661846 http://dx.doi.org/10.4103/0974-8520.96125 |
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