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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
Main Authors: Agrawal, N M, Saffouri, B, Kruss, D M, Callison, D A, Dajani, E Z
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container_end_page 170S
container_issue 11 Suppl
container_start_page 164S
container_title Digestive diseases and sciences
container_volume 30
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.
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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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identifier ISSN: 0163-2116
ispartof Digestive diseases and sciences, 1985-11, Vol.30 (11 Suppl), p.164S-170S
issn 0163-2116
1573-2568
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source SpringerLink Online Journals Archive Complete
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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