Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial
Background. Recurrent episode of allergic rhinitis (AR) is one of the leading illnesses that affects patients. However, there is little research evidence to support pharmacotherapy for AR recurrence. Therefore, this study was designed to explore the efficacy of pharmacotherapy in the control of the...
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description | Background. Recurrent episode of allergic rhinitis (AR) is one of the leading illnesses that affects patients. However, there is little research evidence to support pharmacotherapy for AR recurrence. Therefore, this study was designed to explore the efficacy of pharmacotherapy in the control of the recurrence of AR. Methods. In this study, a multicenter, open-label, randomized, and parallel-arm trial will be conducted at three study centers. A total of 190 subjects aged 18–65 with persistent and moderate-severe AR (Qi deficiency and blood stasis syndrome) will be randomly assigned to receive the modified Yupingfeng nasal spray or mometasone furoate aqueous nasal spray. When subjects’ rhinitis control assessment test (RCAT) score is >21 for two weeks, they will stop taking the medication and enter the follow-up. Once a relapse occurs, the time point will be recorded, and the follow-up stops. The primary outcome is the six-month recurrence rate of AR after intervention withdrawal. The secondary outcomes are the one-month recurrence rate of AR, the RCAT score, the duration of follow-up, the duration of medication, the nasal endoscopic results, and questionnaires to evaluate symptoms, signs, and quality of life. The mechanism outcomes include some indicators that may be associated with AR recurrence. In addition, electrocardiograms and other safety indicators will be applied to evaluate the drug’s safety. Discussion. This is the first study to explore the efficacy of traditional Chinese medicine nasal spray on AR from the perspective of controlling recurrence. The results of this trial may provide valuable clinical evidence for controlling the recurrence of this disease by pharmacotherapy. Trial Registration. This study was registered with registration number ChiCTR2100047053 (Chinese Clinical Trial Registry, https://www.chictr.org.cn/showproj.aspx?proj=127432 on June 7, 2021). |
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Recurrent episode of allergic rhinitis (AR) is one of the leading illnesses that affects patients. However, there is little research evidence to support pharmacotherapy for AR recurrence. Therefore, this study was designed to explore the efficacy of pharmacotherapy in the control of the recurrence of AR. Methods. In this study, a multicenter, open-label, randomized, and parallel-arm trial will be conducted at three study centers. A total of 190 subjects aged 18–65 with persistent and moderate-severe AR (Qi deficiency and blood stasis syndrome) will be randomly assigned to receive the modified Yupingfeng nasal spray or mometasone furoate aqueous nasal spray. When subjects’ rhinitis control assessment test (RCAT) score is >21 for two weeks, they will stop taking the medication and enter the follow-up. Once a relapse occurs, the time point will be recorded, and the follow-up stops. The primary outcome is the six-month recurrence rate of AR after intervention withdrawal. The secondary outcomes are the one-month recurrence rate of AR, the RCAT score, the duration of follow-up, the duration of medication, the nasal endoscopic results, and questionnaires to evaluate symptoms, signs, and quality of life. The mechanism outcomes include some indicators that may be associated with AR recurrence. In addition, electrocardiograms and other safety indicators will be applied to evaluate the drug’s safety. Discussion. This is the first study to explore the efficacy of traditional Chinese medicine nasal spray on AR from the perspective of controlling recurrence. The results of this trial may provide valuable clinical evidence for controlling the recurrence of this disease by pharmacotherapy. Trial Registration. This study was registered with registration number ChiCTR2100047053 (Chinese Clinical Trial Registry, https://www.chictr.org.cn/showproj.aspx?proj=127432 on June 7, 2021).</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2022/4666332</identifier><identifier>PMID: 35990824</identifier><language>eng</language><publisher>New York: Hindawi</publisher><subject>Allergic rhinitis ; Chinese medicine ; Drug therapy ; Hay fever ; Histamine ; Hospitals ; Mental disorders ; Quality of life ; Quality standards ; Rhinitis ; Safety ; Traditional Chinese medicine</subject><ispartof>Evidence-based complementary and alternative medicine, 2022-08, Vol.2022, p.1-10</ispartof><rights>Copyright © 2022 Ting Liu et al.</rights><rights>Copyright © 2022 Ting Liu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Ting Liu et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c382t-4ed214027186f3e27f498d4e5e7e69df0e6523c65e015ac296a5c1c123ebb5063</cites><orcidid>0000-0003-0537-061X ; 0000-0002-5774-2369 ; 0000-0001-9140-9976 ; 0000-0002-8041-0805 ; 0000-0001-8198-9233 ; 0000-0002-6388-7193 ; 0000-0003-3028-4529 ; 0000-0001-9398-7542</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385272/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385272/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><contributor>Zeng, Xiaobin</contributor><contributor>Xiaobin Zeng</contributor><creatorcontrib>Liu, Ting</creatorcontrib><creatorcontrib>Lu, Bing-Qing</creatorcontrib><creatorcontrib>Wang, Dan-Dan</creatorcontrib><creatorcontrib>Liao, Chao</creatorcontrib><creatorcontrib>Chiang, Han-Jen</creatorcontrib><creatorcontrib>Zhang, Rong</creatorcontrib><creatorcontrib>Xi, Yuan</creatorcontrib><creatorcontrib>Tian, Li</creatorcontrib><title>Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial</title><title>Evidence-based complementary and alternative medicine</title><description>Background. Recurrent episode of allergic rhinitis (AR) is one of the leading illnesses that affects patients. However, there is little research evidence to support pharmacotherapy for AR recurrence. Therefore, this study was designed to explore the efficacy of pharmacotherapy in the control of the recurrence of AR. Methods. In this study, a multicenter, open-label, randomized, and parallel-arm trial will be conducted at three study centers. A total of 190 subjects aged 18–65 with persistent and moderate-severe AR (Qi deficiency and blood stasis syndrome) will be randomly assigned to receive the modified Yupingfeng nasal spray or mometasone furoate aqueous nasal spray. When subjects’ rhinitis control assessment test (RCAT) score is >21 for two weeks, they will stop taking the medication and enter the follow-up. Once a relapse occurs, the time point will be recorded, and the follow-up stops. The primary outcome is the six-month recurrence rate of AR after intervention withdrawal. The secondary outcomes are the one-month recurrence rate of AR, the RCAT score, the duration of follow-up, the duration of medication, the nasal endoscopic results, and questionnaires to evaluate symptoms, signs, and quality of life. The mechanism outcomes include some indicators that may be associated with AR recurrence. In addition, electrocardiograms and other safety indicators will be applied to evaluate the drug’s safety. Discussion. This is the first study to explore the efficacy of traditional Chinese medicine nasal spray on AR from the perspective of controlling recurrence. The results of this trial may provide valuable clinical evidence for controlling the recurrence of this disease by pharmacotherapy. Trial Registration. This study was registered with registration number ChiCTR2100047053 (Chinese Clinical Trial Registry, https://www.chictr.org.cn/showproj.aspx?proj=127432 on June 7, 2021).</description><subject>Allergic rhinitis</subject><subject>Chinese medicine</subject><subject>Drug therapy</subject><subject>Hay fever</subject><subject>Histamine</subject><subject>Hospitals</subject><subject>Mental disorders</subject><subject>Quality of life</subject><subject>Quality standards</subject><subject>Rhinitis</subject><subject>Safety</subject><subject>Traditional Chinese medicine</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9ktFu0zAUhiMEYmNwxwNY4gaJhtlOHCdcIFXVGEgdq9ohwVXkOsetJ9cutjOUPSpPg7NWk-CCK1s6nz7_R_6z7DXB7wlh7JxiSs_LqqqKgj7JTgkvSV7Sun76eOffT7IXIdxiTBvO-fPspGBNg2tanma_L5TSUsgBCduhlVAQB-QUunKdVho69KPfa7tRYDfoqwjCoNXeiwFpi2bORu-MSWMUt4CWIHvvwUoYBQvwQYcINj6Ykw-8iJCv4A48oKkx4DdaouVWWx11-IBWse8GtPAuOukMUs4jga56E7VMFvATdL0Hm8_FGswELZPV7fQ9dJOHBxbCi-Q0-dTv0I3XwrzMnilhArw6nmfZt08XN7PP-fz68stsOs9lUdOYl9BRUmLKSV2pAihXZVN3JTDgUDWdwlAxWsiKASZMSNpUgkkiCS1gvWa4Ks6yjwfvvl_voBvDpijt3uud8EPrhG7_nli9bTfurm2KmlFOk-DtUeDdzx5CbHc6SDBGWHB9aCnHrGg45WVC3_yD3rre27TeSJWc1aQZhZMDJb0LwYN6DENwO5amHUvTHkuT8HcHPH1FJ37p_9N_AAWIwyQ</recordid><startdate>20220810</startdate><enddate>20220810</enddate><creator>Liu, Ting</creator><creator>Lu, Bing-Qing</creator><creator>Wang, Dan-Dan</creator><creator>Liao, Chao</creator><creator>Chiang, Han-Jen</creator><creator>Zhang, Rong</creator><creator>Xi, Yuan</creator><creator>Tian, Li</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0537-061X</orcidid><orcidid>https://orcid.org/0000-0002-5774-2369</orcidid><orcidid>https://orcid.org/0000-0001-9140-9976</orcidid><orcidid>https://orcid.org/0000-0002-8041-0805</orcidid><orcidid>https://orcid.org/0000-0001-8198-9233</orcidid><orcidid>https://orcid.org/0000-0002-6388-7193</orcidid><orcidid>https://orcid.org/0000-0003-3028-4529</orcidid><orcidid>https://orcid.org/0000-0001-9398-7542</orcidid></search><sort><creationdate>20220810</creationdate><title>Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial</title><author>Liu, Ting ; Lu, Bing-Qing ; Wang, Dan-Dan ; Liao, Chao ; Chiang, Han-Jen ; Zhang, Rong ; Xi, Yuan ; Tian, Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-4ed214027186f3e27f498d4e5e7e69df0e6523c65e015ac296a5c1c123ebb5063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Allergic rhinitis</topic><topic>Chinese medicine</topic><topic>Drug therapy</topic><topic>Hay fever</topic><topic>Histamine</topic><topic>Hospitals</topic><topic>Mental disorders</topic><topic>Quality of life</topic><topic>Quality standards</topic><topic>Rhinitis</topic><topic>Safety</topic><topic>Traditional Chinese medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Ting</creatorcontrib><creatorcontrib>Lu, Bing-Qing</creatorcontrib><creatorcontrib>Wang, Dan-Dan</creatorcontrib><creatorcontrib>Liao, Chao</creatorcontrib><creatorcontrib>Chiang, Han-Jen</creatorcontrib><creatorcontrib>Zhang, Rong</creatorcontrib><creatorcontrib>Xi, Yuan</creatorcontrib><creatorcontrib>Tian, Li</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Ting</au><au>Lu, Bing-Qing</au><au>Wang, Dan-Dan</au><au>Liao, Chao</au><au>Chiang, Han-Jen</au><au>Zhang, Rong</au><au>Xi, Yuan</au><au>Tian, Li</au><au>Zeng, Xiaobin</au><au>Xiaobin Zeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><date>2022-08-10</date><risdate>2022</risdate><volume>2022</volume><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Background. Recurrent episode of allergic rhinitis (AR) is one of the leading illnesses that affects patients. However, there is little research evidence to support pharmacotherapy for AR recurrence. Therefore, this study was designed to explore the efficacy of pharmacotherapy in the control of the recurrence of AR. Methods. In this study, a multicenter, open-label, randomized, and parallel-arm trial will be conducted at three study centers. A total of 190 subjects aged 18–65 with persistent and moderate-severe AR (Qi deficiency and blood stasis syndrome) will be randomly assigned to receive the modified Yupingfeng nasal spray or mometasone furoate aqueous nasal spray. When subjects’ rhinitis control assessment test (RCAT) score is >21 for two weeks, they will stop taking the medication and enter the follow-up. Once a relapse occurs, the time point will be recorded, and the follow-up stops. The primary outcome is the six-month recurrence rate of AR after intervention withdrawal. The secondary outcomes are the one-month recurrence rate of AR, the RCAT score, the duration of follow-up, the duration of medication, the nasal endoscopic results, and questionnaires to evaluate symptoms, signs, and quality of life. The mechanism outcomes include some indicators that may be associated with AR recurrence. In addition, electrocardiograms and other safety indicators will be applied to evaluate the drug’s safety. Discussion. This is the first study to explore the efficacy of traditional Chinese medicine nasal spray on AR from the perspective of controlling recurrence. The results of this trial may provide valuable clinical evidence for controlling the recurrence of this disease by pharmacotherapy. Trial Registration. This study was registered with registration number ChiCTR2100047053 (Chinese Clinical Trial Registry, https://www.chictr.org.cn/showproj.aspx?proj=127432 on June 7, 2021).</abstract><cop>New York</cop><pub>Hindawi</pub><pmid>35990824</pmid><doi>10.1155/2022/4666332</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-0537-061X</orcidid><orcidid>https://orcid.org/0000-0002-5774-2369</orcidid><orcidid>https://orcid.org/0000-0001-9140-9976</orcidid><orcidid>https://orcid.org/0000-0002-8041-0805</orcidid><orcidid>https://orcid.org/0000-0001-8198-9233</orcidid><orcidid>https://orcid.org/0000-0002-6388-7193</orcidid><orcidid>https://orcid.org/0000-0003-3028-4529</orcidid><orcidid>https://orcid.org/0000-0001-9398-7542</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Allergic rhinitis Chinese medicine Drug therapy Hay fever Histamine Hospitals Mental disorders Quality of life Quality standards Rhinitis Safety Traditional Chinese medicine |
title | Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial |
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