Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/110340
DC Field | Value | Language |
---|---|---|
dc.contributor | College of Professional and Continuing Education | - |
dc.creator | Sum, CH | - |
dc.creator | Li, TW | - |
dc.creator | Zhang, HW | - |
dc.creator | Hung, HY | - |
dc.creator | Fong, BF | - |
dc.creator | Lin, WL | - |
dc.creator | Chow, TY | - |
dc.creator | Leung, KC | - |
dc.creator | Lo, CW | - |
dc.creator | Chia, CP | - |
dc.creator | Chan, KL | - |
dc.creator | Lin, ZX | - |
dc.date.accessioned | 2024-12-03T03:34:04Z | - |
dc.date.available | 2024-12-03T03:34:04Z | - |
dc.identifier.uri | http://hdl.handle.net/10397/110340 | - |
dc.language.iso | en | en_US |
dc.publisher | Frontiers Research Foundation | en_US |
dc.rights | © 2024 Sum, Li, Zhang, Hung, Fong, Lin, Chow, Leung, Lo, Chia, Chan and Lin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. | en_US |
dc.rights | The following publication Sum CH, Li TW, Zhang H, Hung HY, Fong BYF, Lin WL, Chow TY, Leung KC, Lo CW, Chia CP, Chan KL and Lin Z-x (2024) Assessing the efficacy and safety of Yinqiao powder-maxing Ganshi decoction in the treatment of the major symptoms of mild and moderate COVID-19 by telemedicine–study protocol for a randomized, double-blind, placebo-controlled trial. Front. Pharmacol. 14:1261338 is available at https://dx.doi.org/10.3389/fphar.2023.1261338. | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | Chinese medicine | en_US |
dc.subject | Yinqiao Powder | en_US |
dc.subject | Maxing Ganshi decoction | en_US |
dc.subject | Randomized control trial | en_US |
dc.subject | Clinical trial | en_US |
dc.title | Assessing the efficacy and safety of Yinqiao powder-maxing Ganshi decoction in the treatment of the major symptoms of mild and moderate COVID-19 by telemedicine-study protocol for a randomized, double-blind, placebo-controlled trial | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.volume | 14 | - |
dc.identifier.doi | 10.3389/fphar.2023.1261338 | - |
dcterms.abstract | Background: The Coronavirus disease 2019 (COVID-19) is the largest global epidemic in recent time. Chinese medicine has been recognized by the World Health Organization as an effective treatment for COVID-19, but there is still a lack of high-quality randomized, double-blind trials using placebo as the control to support its application, which may hinder its further promotion locally and internationally. | - |
dcterms.abstract | Objectives: This study will evaluate the efficacy and safety of Yinqiao Powder-Maxing Ganshi Decoction with variation in relieving major symptoms of mild and moderate COVID-19 by telemedicine. | - |
dcterms.abstract | Methods and design: This clinical study is a randomized, double-blind, placebo-controlled trial that applies telemedicine to evaluate the efficacy and safety of Yinqiao Powder-Maxing Ganshi Decoction in the treatment of mild and moderate COVID-19. Eligible subjects will be randomly divided into either treatment or placebo groups for up to 14 days after stratification according to age (A:18-49, B:50-65) and the number of vaccinations (a: >= 3 doses, b: <= 2 doses). The treatment group will receive Yinqiao Powder-Maxing Ganshi Decoction granules along with certain variation based on their symptoms, and the placebo group will receive the same amount of placebo granules. Subjects will be prescribed different additions based on their symptoms and pathogenesis at the inclusion. The oral temperature, oximeter, result of rapid antigen test and symptom score will be recorded by subjects until they have stopped the medication. Subjects are required to have follow-up assessment by video-conference on days 7, 14 and 35. The time for the body temperature returning to normal will be used as the primary outcome. | - |
dcterms.abstract | Discussion: This trial will provide scientific evidence on the use of Yinqiao Powder-Maxing Ganshi Decoction for the treatment of COVID-19, and the results would help raise the awareness in Hong Kong and the international community on the use of Chinese herbal medicine for treating COVID-19. | - |
dcterms.abstract | Clinical Trial Registration: clinicaltrials.gov, identifier NCT05787327. | - |
dcterms.accessRights | open access | en_US |
dcterms.bibliographicCitation | Frontiers in pharmacology, 2024, v. 14, 1261338 | - |
dcterms.isPartOf | Frontiers in pharmacology | - |
dcterms.issued | 2024 | - |
dc.identifier.isi | WOS:001154672700001 | - |
dc.identifier.pmid | 38259270 | - |
dc.identifier.eissn | 1663-9812 | - |
dc.identifier.artn | 1261338 | - |
dc.description.validate | 202412 bcrc | - |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | OA_Scopus/WOS | en_US |
dc.description.fundingSource | Others | en_US |
dc.description.fundingText | Chinese Medicine Development Fund of the Hong Kong Special Administrative Region Government | en_US |
dc.description.pubStatus | Published | en_US |
dc.description.oaCategory | CC | en_US |
Appears in Collections: | Journal/Magazine Article |
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File | Description | Size | Format | |
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fphar-14-1261338.pdf | 773.03 kB | Adobe PDF | View/Open |
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