Triletide in a cimetidine-controlled clinical evaluation in duodenal ulcer patients

A controlled study was carried out in 20 out-patients with endoscopically confirmed active duodenal ulcer to compare the effectiveness and tolerance of a new cytoprotective agent, triletide, with an established antisecretory agent, cimetidine. Patients were allocated at random to receive 8-weeks...

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Bibliographische Detailangaben
Veröffentlicht in:Interim guidelines for the control of infections with Vero cytotoxin producing Escherichia coli (VTEC). Subcommittee of the PHLS Working Group on Vero cytotoxin producing Escherichia coli (VTEC). - 1995. - 4(1985), 3 Spec No vom: 15., Seite 177-81
1. Verfasser: Primbs, P (VerfasserIn)
Format: Aufsatz
Sprache:English
Veröffentlicht: 1985
Zugriff auf das übergeordnete Werk:Interim guidelines for the control of infections with Vero cytotoxin producing Escherichia coli (VTEC). Subcommittee of the PHLS Working Group on Vero cytotoxin producing Escherichia coli (VTEC)
Schlagworte:Clinical Trial Comparative Study Journal Article Randomized Controlled Trial Antacids Anti-Ulcer Agents Oligopeptides triletide 50Q6LI773L Cimetidine 80061L1WGD
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245 1 0 |a Triletide in a cimetidine-controlled clinical evaluation in duodenal ulcer patients 
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520 |a A controlled study was carried out in 20 out-patients with endoscopically confirmed active duodenal ulcer to compare the effectiveness and tolerance of a new cytoprotective agent, triletide, with an established antisecretory agent, cimetidine. Patients were allocated at random to receive 8-weeks' treatment with either 1.5 g triletide per day or 1.2 g cimetidine per day. The results showed that all patients experienced improvement of the ulcer condition by the end of treatment, the vast majority being found endoscopically healed. There was no statistically significant difference between the groups. At the same time, the intensity of heartburn and epigastric pain, as well as the mean antacid intake, decreased significantly with both drugs, almost to the same extent. A significant relief of symptoms was already apparent by the end of 2 weeks of treatment, except for heartburn in the cimetidine group which did not show improvement until the fourth week. There were no complaints of possible side-effects with either treatment and no evidence of any significant changes in blood pressure, heart rate or routine haematology and haematochemistry investigations 
650 4 |a Clinical Trial 
650 4 |a Comparative Study 
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650 4 |a Randomized Controlled Trial 
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650 7 |a Oligopeptides  |2 NLM 
650 7 |a triletide  |2 NLM 
650 7 |a 50Q6LI773L  |2 NLM 
650 7 |a Cimetidine  |2 NLM 
650 7 |a 80061L1WGD  |2 NLM 
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952 |d 4  |j 1985  |e 3 Spec No  |b 15  |h 177-81