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Healing of benign gastric ulcer. A placebo-controlled comparison of two dosage regimens of misoprostol, a synthetic analog of prostaglandin E1
Misoprostol, a synthetic prostaglandin E1 methyl ester analog with gastric antisecretory and cytoprotective properties, prevents the development of acute experimental gastric and duodenal ulcers in various animal models. This study was designed as a multicenter randomized double-blind parallel-group...
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Published in: | Digestive diseases and sciences 1985-11, Vol.30 (11 Suppl), p.164S-170S |
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creator | Agrawal, N M Saffouri, B Kruss, D M Callison, D A Dajani, E Z |
description | Misoprostol, a synthetic prostaglandin E1 methyl ester analog with gastric antisecretory and cytoprotective properties, prevents the development of acute experimental gastric and duodenal ulcers in various animal models. This study was designed as a multicenter randomized double-blind parallel-group comparison of the effects of two dosage strengths (25 and 100 micrograms q.i.d.) of orally-administered misoprostol and placebo on the healing of endoscopically-proven benign gastric ulcer in 299 out-patients. Safety was evaluated by comparison of pre- and post-treatment physical examinations, clinical laboratory tests, gastric antral biopsies and monitoring of adverse experiences. A statistically significant difference in gastric ulcer healing rate was seen at eight weeks among the treatment groups in the Intent-to-Treat Cohort: misoprostol 100 micrograms (62.0%), misoprostol 25 micrograms (50.0%), placebo (44.7%). The proportion of subjects healed in up to eight weeks of treatment was greatest in the misoprostol 100 micrograms group in all cohorts. Ulcer pain decreased in all treatment groups in successive weeks and there were no statistical differences among any of the three treatment groups. Diarrhea was the most frequently reported adverse experience: misoprostol 100 micrograms (9.8%), misoprostol 25 micrograms (7.7%), placebo (1.9%). The diarrhea was mild and self-limiting despite continued use of misoprostol. Overall evaluation of gastric antral biopsies showed no adverse changes in the morphology of the antral mucosa. We conclude that misoprostol 100 micrograms q.i.d. for up to eight weeks is safe and effective in the treatment of benign gastric ulcer. |
doi_str_mv | 10.1007/BF01309404 |
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Safety was evaluated by comparison of pre- and post-treatment physical examinations, clinical laboratory tests, gastric antral biopsies and monitoring of adverse experiences. A statistically significant difference in gastric ulcer healing rate was seen at eight weeks among the treatment groups in the Intent-to-Treat Cohort: misoprostol 100 micrograms (62.0%), misoprostol 25 micrograms (50.0%), placebo (44.7%). The proportion of subjects healed in up to eight weeks of treatment was greatest in the misoprostol 100 micrograms group in all cohorts. Ulcer pain decreased in all treatment groups in successive weeks and there were no statistical differences among any of the three treatment groups. Diarrhea was the most frequently reported adverse experience: misoprostol 100 micrograms (9.8%), misoprostol 25 micrograms (7.7%), placebo (1.9%). The diarrhea was mild and self-limiting despite continued use of misoprostol. Overall evaluation of gastric antral biopsies showed no adverse changes in the morphology of the antral mucosa. We conclude that misoprostol 100 micrograms q.i.d. for up to eight weeks is safe and effective in the treatment of benign gastric ulcer.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/BF01309404</identifier><identifier>PMID: 3932050</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Alprostadil - administration & dosage ; Alprostadil - adverse effects ; Alprostadil - analogs & derivatives ; Alprostadil - therapeutic use ; Anti-Ulcer Agents - administration & dosage ; Anti-Ulcer Agents - adverse effects ; Anti-Ulcer Agents - therapeutic use ; Clinical Trials as Topic ; Double-Blind Method ; Drug Administration Schedule ; Female ; Gastroscopy ; Humans ; Male ; Middle Aged ; Misoprostol ; Placebos ; Pyloric Antrum - pathology ; Random Allocation ; Stomach Ulcer - drug therapy ; Stomach Ulcer - pathology</subject><ispartof>Digestive diseases and sciences, 1985-11, Vol.30 (11 Suppl), p.164S-170S</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c156t-ac54600cc57477ed3b73b6f91ecb76c589f5432f88e289ae54901ee2c24d96383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3932050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Agrawal, N M</creatorcontrib><creatorcontrib>Saffouri, B</creatorcontrib><creatorcontrib>Kruss, D M</creatorcontrib><creatorcontrib>Callison, D A</creatorcontrib><creatorcontrib>Dajani, E Z</creatorcontrib><title>Healing of benign gastric ulcer. A placebo-controlled comparison of two dosage regimens of misoprostol, a synthetic analog of prostaglandin E1</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><description>Misoprostol, a synthetic prostaglandin E1 methyl ester analog with gastric antisecretory and cytoprotective properties, prevents the development of acute experimental gastric and duodenal ulcers in various animal models. This study was designed as a multicenter randomized double-blind parallel-group comparison of the effects of two dosage strengths (25 and 100 micrograms q.i.d.) of orally-administered misoprostol and placebo on the healing of endoscopically-proven benign gastric ulcer in 299 out-patients. Safety was evaluated by comparison of pre- and post-treatment physical examinations, clinical laboratory tests, gastric antral biopsies and monitoring of adverse experiences. A statistically significant difference in gastric ulcer healing rate was seen at eight weeks among the treatment groups in the Intent-to-Treat Cohort: misoprostol 100 micrograms (62.0%), misoprostol 25 micrograms (50.0%), placebo (44.7%). The proportion of subjects healed in up to eight weeks of treatment was greatest in the misoprostol 100 micrograms group in all cohorts. Ulcer pain decreased in all treatment groups in successive weeks and there were no statistical differences among any of the three treatment groups. Diarrhea was the most frequently reported adverse experience: misoprostol 100 micrograms (9.8%), misoprostol 25 micrograms (7.7%), placebo (1.9%). The diarrhea was mild and self-limiting despite continued use of misoprostol. Overall evaluation of gastric antral biopsies showed no adverse changes in the morphology of the antral mucosa. We conclude that misoprostol 100 micrograms q.i.d. for up to eight weeks is safe and effective in the treatment of benign gastric ulcer.</description><subject>Adult</subject><subject>Aged</subject><subject>Alprostadil - administration & dosage</subject><subject>Alprostadil - adverse effects</subject><subject>Alprostadil - analogs & derivatives</subject><subject>Alprostadil - therapeutic use</subject><subject>Anti-Ulcer Agents - administration & dosage</subject><subject>Anti-Ulcer Agents - adverse effects</subject><subject>Anti-Ulcer Agents - therapeutic use</subject><subject>Clinical Trials as Topic</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Gastroscopy</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Misoprostol</subject><subject>Placebos</subject><subject>Pyloric Antrum - pathology</subject><subject>Random Allocation</subject><subject>Stomach Ulcer - drug therapy</subject><subject>Stomach Ulcer - pathology</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><recordid>eNpFkE9P3DAQxS1UtCx_Lr0j-dQDIjC2Yzs5AmJLJSQucI4cZxJSOfbWzqraL8Fnxsuu2tOMZt68-ekR8p3BDQPQt_crYALqEsojsmRSi4JLVX0jS2Aq94ypE3Ka0m8AqDVTC7IQteAgYUk-ntC40Q809LRFPw6eDibNcbR04yzGG3pH185YbENhg59jcA47asO0NnFMwe8O57-BdiGZAWnEYZzQp914yvt1DGkO7poamrZ-fsc5OxtvXPh6-bU2gzO-Gz19ZOfkuDcu4cWhnpG31ePrw1Px_PLz18Pdc2GZVHNhrCwVgLVSl1pjJ1otWtXXDG2rlZVV3ctS8L6qkFe1QVnWwBC55WVXK1GJM_Jj75sB_mwwzU2GtegyCIZNarQqOQeusvBqL7SZNEXsm3UcJxO3DYNmF37zP_wsvjy4btoJu3_SQ9riE_wigDc</recordid><startdate>198511</startdate><enddate>198511</enddate><creator>Agrawal, N M</creator><creator>Saffouri, B</creator><creator>Kruss, D M</creator><creator>Callison, D A</creator><creator>Dajani, E Z</creator><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>7X8</scope></search><sort><creationdate>198511</creationdate><title>Healing of benign gastric ulcer. A placebo-controlled comparison of two dosage regimens of misoprostol, a synthetic analog of prostaglandin E1</title><author>Agrawal, N M ; Saffouri, B ; Kruss, D M ; Callison, D A ; Dajani, E Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c156t-ac54600cc57477ed3b73b6f91ecb76c589f5432f88e289ae54901ee2c24d96383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alprostadil - administration & dosage</topic><topic>Alprostadil - adverse effects</topic><topic>Alprostadil - analogs & derivatives</topic><topic>Alprostadil - therapeutic use</topic><topic>Anti-Ulcer Agents - administration & dosage</topic><topic>Anti-Ulcer Agents - adverse effects</topic><topic>Anti-Ulcer Agents - therapeutic use</topic><topic>Clinical Trials as Topic</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Gastroscopy</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Misoprostol</topic><topic>Placebos</topic><topic>Pyloric Antrum - pathology</topic><topic>Random Allocation</topic><topic>Stomach Ulcer - drug therapy</topic><topic>Stomach Ulcer - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agrawal, N M</creatorcontrib><creatorcontrib>Saffouri, B</creatorcontrib><creatorcontrib>Kruss, D M</creatorcontrib><creatorcontrib>Callison, D A</creatorcontrib><creatorcontrib>Dajani, E Z</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agrawal, N M</au><au>Saffouri, B</au><au>Kruss, D M</au><au>Callison, D A</au><au>Dajani, E Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Healing of benign gastric ulcer. A placebo-controlled comparison of two dosage regimens of misoprostol, a synthetic analog of prostaglandin E1</atitle><jtitle>Digestive diseases and sciences</jtitle><addtitle>Dig Dis Sci</addtitle><date>1985-11</date><risdate>1985</risdate><volume>30</volume><issue>11 Suppl</issue><spage>164S</spage><epage>170S</epage><pages>164S-170S</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><abstract>Misoprostol, a synthetic prostaglandin E1 methyl ester analog with gastric antisecretory and cytoprotective properties, prevents the development of acute experimental gastric and duodenal ulcers in various animal models. This study was designed as a multicenter randomized double-blind parallel-group comparison of the effects of two dosage strengths (25 and 100 micrograms q.i.d.) of orally-administered misoprostol and placebo on the healing of endoscopically-proven benign gastric ulcer in 299 out-patients. Safety was evaluated by comparison of pre- and post-treatment physical examinations, clinical laboratory tests, gastric antral biopsies and monitoring of adverse experiences. A statistically significant difference in gastric ulcer healing rate was seen at eight weeks among the treatment groups in the Intent-to-Treat Cohort: misoprostol 100 micrograms (62.0%), misoprostol 25 micrograms (50.0%), placebo (44.7%). The proportion of subjects healed in up to eight weeks of treatment was greatest in the misoprostol 100 micrograms group in all cohorts. Ulcer pain decreased in all treatment groups in successive weeks and there were no statistical differences among any of the three treatment groups. Diarrhea was the most frequently reported adverse experience: misoprostol 100 micrograms (9.8%), misoprostol 25 micrograms (7.7%), placebo (1.9%). The diarrhea was mild and self-limiting despite continued use of misoprostol. Overall evaluation of gastric antral biopsies showed no adverse changes in the morphology of the antral mucosa. We conclude that misoprostol 100 micrograms q.i.d. for up to eight weeks is safe and effective in the treatment of benign gastric ulcer.</abstract><cop>United States</cop><pmid>3932050</pmid><doi>10.1007/BF01309404</doi></addata></record> |
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subjects | Adult Aged Alprostadil - administration & dosage Alprostadil - adverse effects Alprostadil - analogs & derivatives Alprostadil - therapeutic use Anti-Ulcer Agents - administration & dosage Anti-Ulcer Agents - adverse effects Anti-Ulcer Agents - therapeutic use Clinical Trials as Topic Double-Blind Method Drug Administration Schedule Female Gastroscopy Humans Male Middle Aged Misoprostol Placebos Pyloric Antrum - pathology Random Allocation Stomach Ulcer - drug therapy Stomach Ulcer - pathology |
title | Healing of benign gastric ulcer. A placebo-controlled comparison of two dosage regimens of misoprostol, a synthetic analog of prostaglandin E1 |
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