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Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial
With the development of traditional Chinese medicine research, berberine has shown good efficacy and safety in the eradication of Helicobacter pylori (H. pylori). The present study aimed to evaluate the efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for the i...
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Published in: | Chinese medical journal 2023-07, Vol.136 (14), p.1690-1698 |
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description | With the development of traditional Chinese medicine research, berberine has shown good efficacy and safety in the eradication of Helicobacter pylori (H. pylori). The present study aimed to evaluate the efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for the initial treatment of H. pylori.
This study was a single-center, open-label, parallel, randomized controlled clinical trial. Patients with H. pylori infection were randomly (1:1:1) assigned to receive berberine triple therapy (berberine 500 mg, amoxicillin 1000 mg, vonoprazan 20 mg, A group), vonoprazan quadruple therapy (vonoprazan 20 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, B group), or rabeprazole quadruple therapy (rabeprazole 10 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, C group). The drugs were taken twice daily for 14 days. The main outcome was the H. pylori eradication rate. The secondary outcomes were symptom improvement rate, patient compliance, and incidence of adverse events. Furthermore, factors affecting the eradication rate of H. pylori were further analyzed.
A total of 300 H. pylori-infected patients were included in this study, and 263 patients completed the study. An intention-to-treat (ITT) analysis showed that the eradication rates of H. pylori in berberine triple therapy, vonoprazan quadruple therapy, and rabeprazole quadruple therapy were 70.0% (70/100), 77.0% (77/100), and 69.0% (69/100), respectively. The per-protocol (PP) analysis showed that the eradication rates of H. pylori in these three groups were 81.4% (70/86), 86.5% (77/89), and 78.4% (69/88), respectively. Both ITT analysis and PP analysis showed that the H. pylori eradication rate did not significantly differ among the three groups (P >0.05). In addition, the symptom improvement rate, overall adverse reaction rate, and patient compliance were similar among the three groups (P >0.05).
The efficacy of berberine triple therapy for H. pylori initial treatment was comparable to that of vonoprazan quadruple therapy and rabeprazole quadruple therapy, and it was well tolerated. It could be used as one choice of H. pylori initial treatment. |
doi_str_mv | 10.1097/CM9.0000000000002696 |
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This study was a single-center, open-label, parallel, randomized controlled clinical trial. Patients with H. pylori infection were randomly (1:1:1) assigned to receive berberine triple therapy (berberine 500 mg, amoxicillin 1000 mg, vonoprazan 20 mg, A group), vonoprazan quadruple therapy (vonoprazan 20 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, B group), or rabeprazole quadruple therapy (rabeprazole 10 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, C group). The drugs were taken twice daily for 14 days. The main outcome was the H. pylori eradication rate. The secondary outcomes were symptom improvement rate, patient compliance, and incidence of adverse events. Furthermore, factors affecting the eradication rate of H. pylori were further analyzed.
A total of 300 H. pylori-infected patients were included in this study, and 263 patients completed the study. An intention-to-treat (ITT) analysis showed that the eradication rates of H. pylori in berberine triple therapy, vonoprazan quadruple therapy, and rabeprazole quadruple therapy were 70.0% (70/100), 77.0% (77/100), and 69.0% (69/100), respectively. The per-protocol (PP) analysis showed that the eradication rates of H. pylori in these three groups were 81.4% (70/86), 86.5% (77/89), and 78.4% (69/88), respectively. Both ITT analysis and PP analysis showed that the H. pylori eradication rate did not significantly differ among the three groups (P >0.05). In addition, the symptom improvement rate, overall adverse reaction rate, and patient compliance were similar among the three groups (P >0.05).
The efficacy of berberine triple therapy for H. pylori initial treatment was comparable to that of vonoprazan quadruple therapy and rabeprazole quadruple therapy, and it was well tolerated. It could be used as one choice of H. pylori initial treatment.</description><identifier>ISSN: 0366-6999</identifier><identifier>ISSN: 2542-5641</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/CM9.0000000000002696</identifier><identifier>PMID: 37469024</identifier><language>eng</language><publisher>China: Lippincott Williams & Wilkins</publisher><subject>Acids ; Amoxicillin - therapeutic use ; Anti-Bacterial Agents ; Antibiotics ; Berberine - therapeutic use ; Bismuth ; Clarithromycin - therapeutic use ; Clinical trials ; Drug resistance ; Drug Therapy, Combination ; Drug withdrawal ; Enrollments ; Helicobacter Infections - drug therapy ; Helicobacter pylori ; Hospitals ; Humans ; Infections ; Original ; Penicillin ; Pharmaceutical industry ; Proton Pump Inhibitors - therapeutic use ; Rabeprazole - therapeutic use ; Treatment Outcome</subject><ispartof>Chinese medical journal, 2023-07, Vol.136 (14), p.1690-1698</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license.</rights><rights>Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5487-b1ac625f2097c5b3d256a4a5427b7bb8afaeea0d51c07f9616df65d0166d9a2b3</citedby><cites>FETCH-LOGICAL-c5487-b1ac625f2097c5b3d256a4a5427b7bb8afaeea0d51c07f9616df65d0166d9a2b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344537/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2839647891?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,36989,44565,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37469024$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Shasha</creatorcontrib><creatorcontrib>Shen, Weina</creatorcontrib><creatorcontrib>Liu, Yuhuan</creatorcontrib><creatorcontrib>Dong, Qiang</creatorcontrib><creatorcontrib>Shi, Yongquan</creatorcontrib><title>Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial</title><title>Chinese medical journal</title><addtitle>Chin Med J (Engl)</addtitle><description>With the development of traditional Chinese medicine research, berberine has shown good efficacy and safety in the eradication of Helicobacter pylori (H. pylori). The present study aimed to evaluate the efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for the initial treatment of H. pylori.
This study was a single-center, open-label, parallel, randomized controlled clinical trial. Patients with H. pylori infection were randomly (1:1:1) assigned to receive berberine triple therapy (berberine 500 mg, amoxicillin 1000 mg, vonoprazan 20 mg, A group), vonoprazan quadruple therapy (vonoprazan 20 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, B group), or rabeprazole quadruple therapy (rabeprazole 10 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, C group). The drugs were taken twice daily for 14 days. The main outcome was the H. pylori eradication rate. The secondary outcomes were symptom improvement rate, patient compliance, and incidence of adverse events. Furthermore, factors affecting the eradication rate of H. pylori were further analyzed.
A total of 300 H. pylori-infected patients were included in this study, and 263 patients completed the study. An intention-to-treat (ITT) analysis showed that the eradication rates of H. pylori in berberine triple therapy, vonoprazan quadruple therapy, and rabeprazole quadruple therapy were 70.0% (70/100), 77.0% (77/100), and 69.0% (69/100), respectively. The per-protocol (PP) analysis showed that the eradication rates of H. pylori in these three groups were 81.4% (70/86), 86.5% (77/89), and 78.4% (69/88), respectively. Both ITT analysis and PP analysis showed that the H. pylori eradication rate did not significantly differ among the three groups (P >0.05). In addition, the symptom improvement rate, overall adverse reaction rate, and patient compliance were similar among the three groups (P >0.05).
The efficacy of berberine triple therapy for H. pylori initial treatment was comparable to that of vonoprazan quadruple therapy and rabeprazole quadruple therapy, and it was well tolerated. It could be used as one choice of H. pylori initial treatment.</description><subject>Acids</subject><subject>Amoxicillin - therapeutic use</subject><subject>Anti-Bacterial Agents</subject><subject>Antibiotics</subject><subject>Berberine - therapeutic use</subject><subject>Bismuth</subject><subject>Clarithromycin - therapeutic use</subject><subject>Clinical trials</subject><subject>Drug resistance</subject><subject>Drug Therapy, Combination</subject><subject>Drug withdrawal</subject><subject>Enrollments</subject><subject>Helicobacter Infections - drug therapy</subject><subject>Helicobacter pylori</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Infections</subject><subject>Original</subject><subject>Penicillin</subject><subject>Pharmaceutical industry</subject><subject>Proton Pump Inhibitors - therapeutic use</subject><subject>Rabeprazole - therapeutic use</subject><subject>Treatment Outcome</subject><issn>0366-6999</issn><issn>2542-5641</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkt1uFCEUxydGY2v1DYwh8caLTmUYPhZvmmZTbZMab_SaHBjYZWVgZGZbt0_jo8ru1tqWkHAC__M7H5yqetvgkwZL8XH-VZ7gB4twyZ9Vh4RRUjNOm-fVIW45r7mU8qB6NY6romFM8JfVQSsol5jQw-rPuXPegNkgiB0awdlpg5JDU_ZDsGha2gzDBpkUJ_DRxwXSNpftoz1G0Kff3vgQfDze-V-nmIYMtxCRSxld2OBN0mAmm9GwCSl7VCCTh1ACWJh6G6dP6Azl4px6f2u7XaScQihmyQHC6-qFgzDaN3fnUfXj8_n3-UV99e3L5fzsqjaMzkStGzCcMEdKawzTbUcYBwqlGUILrWfgwFrAHWsMFk7yhneOsw43nHcSiG6Pqss9t0uwUkP2PeSNSuDV7iLlhYI8eROsYpph7ACLEopqV6zGGcawppITbnlhne5Zw1r3tjOlygzhEfTxS_RLtUjXqsEtpawVhfDhjpDTr7UdJ9X70dgQINq0HhWZ0fJ9XNKt9P0T6Sqtcyy9KqpWcipmsikquleZnMYxW3efTYPVdp5UmSf1dJ6K27uHldw7_Rug_9ybFMovjz_D-sZmtbQQpuWWR2Tb4ppg0mJBMK63aNH-BQf32VE</recordid><startdate>20230720</startdate><enddate>20230720</enddate><creator>Chen, Shasha</creator><creator>Shen, Weina</creator><creator>Liu, Yuhuan</creator><creator>Dong, Qiang</creator><creator>Shi, Yongquan</creator><general>Lippincott Williams & Wilkins</general><general>Lippincott Williams & Wilkins Ovid Technologies</general><general>Wolters Kluwer</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230720</creationdate><title>Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial</title><author>Chen, Shasha ; Shen, Weina ; Liu, Yuhuan ; Dong, Qiang ; Shi, Yongquan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5487-b1ac625f2097c5b3d256a4a5427b7bb8afaeea0d51c07f9616df65d0166d9a2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acids</topic><topic>Amoxicillin - therapeutic use</topic><topic>Anti-Bacterial Agents</topic><topic>Antibiotics</topic><topic>Berberine - therapeutic use</topic><topic>Bismuth</topic><topic>Clarithromycin - therapeutic use</topic><topic>Clinical trials</topic><topic>Drug resistance</topic><topic>Drug Therapy, Combination</topic><topic>Drug withdrawal</topic><topic>Enrollments</topic><topic>Helicobacter Infections - drug therapy</topic><topic>Helicobacter pylori</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Infections</topic><topic>Original</topic><topic>Penicillin</topic><topic>Pharmaceutical industry</topic><topic>Proton Pump Inhibitors - therapeutic use</topic><topic>Rabeprazole - therapeutic use</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Shasha</creatorcontrib><creatorcontrib>Shen, Weina</creatorcontrib><creatorcontrib>Liu, Yuhuan</creatorcontrib><creatorcontrib>Dong, Qiang</creatorcontrib><creatorcontrib>Shi, Yongquan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</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 Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Shasha</au><au>Shen, Weina</au><au>Liu, Yuhuan</au><au>Dong, Qiang</au><au>Shi, Yongquan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chin Med J (Engl)</addtitle><date>2023-07-20</date><risdate>2023</risdate><volume>136</volume><issue>14</issue><spage>1690</spage><epage>1698</epage><pages>1690-1698</pages><issn>0366-6999</issn><issn>2542-5641</issn><eissn>2542-5641</eissn><abstract>With the development of traditional Chinese medicine research, berberine has shown good efficacy and safety in the eradication of Helicobacter pylori (H. pylori). The present study aimed to evaluate the efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for the initial treatment of H. pylori.
This study was a single-center, open-label, parallel, randomized controlled clinical trial. Patients with H. pylori infection were randomly (1:1:1) assigned to receive berberine triple therapy (berberine 500 mg, amoxicillin 1000 mg, vonoprazan 20 mg, A group), vonoprazan quadruple therapy (vonoprazan 20 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, B group), or rabeprazole quadruple therapy (rabeprazole 10 mg, amoxicillin 1000 mg, clarithromycin 500 mg, colloidal bismuth tartrate 220 mg, C group). The drugs were taken twice daily for 14 days. The main outcome was the H. pylori eradication rate. The secondary outcomes were symptom improvement rate, patient compliance, and incidence of adverse events. Furthermore, factors affecting the eradication rate of H. pylori were further analyzed.
A total of 300 H. pylori-infected patients were included in this study, and 263 patients completed the study. An intention-to-treat (ITT) analysis showed that the eradication rates of H. pylori in berberine triple therapy, vonoprazan quadruple therapy, and rabeprazole quadruple therapy were 70.0% (70/100), 77.0% (77/100), and 69.0% (69/100), respectively. The per-protocol (PP) analysis showed that the eradication rates of H. pylori in these three groups were 81.4% (70/86), 86.5% (77/89), and 78.4% (69/88), respectively. Both ITT analysis and PP analysis showed that the H. pylori eradication rate did not significantly differ among the three groups (P >0.05). In addition, the symptom improvement rate, overall adverse reaction rate, and patient compliance were similar among the three groups (P >0.05).
The efficacy of berberine triple therapy for H. pylori initial treatment was comparable to that of vonoprazan quadruple therapy and rabeprazole quadruple therapy, and it was well tolerated. It could be used as one choice of H. pylori initial treatment.</abstract><cop>China</cop><pub>Lippincott Williams & Wilkins</pub><pmid>37469024</pmid><doi>10.1097/CM9.0000000000002696</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acids Amoxicillin - therapeutic use Anti-Bacterial Agents Antibiotics Berberine - therapeutic use Bismuth Clarithromycin - therapeutic use Clinical trials Drug resistance Drug Therapy, Combination Drug withdrawal Enrollments Helicobacter Infections - drug therapy Helicobacter pylori Hospitals Humans Infections Original Penicillin Pharmaceutical industry Proton Pump Inhibitors - therapeutic use Rabeprazole - therapeutic use Treatment Outcome |
title | Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial |
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