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01000naa a22002652 4500 |
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NLM038850389 |
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DE-627 |
| 005 |
20231221143907.0 |
| 007 |
tu |
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231221s1985 xx ||||| 00| ||eng c |
| 028 |
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|a pubmed24n0130.xml
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|a (DE-627)NLM038850389
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|a (NLM)3903787
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a eng
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| 100 |
1 |
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|a Gandolfi, L
|e verfasserin
|4 aut
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| 245 |
1 |
0 |
|a Triletide and ranitidine for the management of chronic duodenal ulcer
|b a controlled clinical investigation
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| 264 |
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1 |
|c 1985
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| 336 |
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|a Text
|b txt
|2 rdacontent
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| 337 |
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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| 338 |
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|a Band
|b nc
|2 rdacarrier
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| 500 |
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|a Date Completed 18.12.1985
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| 500 |
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|a Date Revised 21.11.2013
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| 500 |
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|a published: Print
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| 500 |
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|a Citation Status MEDLINE
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| 520 |
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|a Twenty out-patients with active, chronic duodenal ulcer were treated over a period of 6 weeks with either 0.6 g ranitidine per day or 2 g triletide per day, a new synthetic tripeptide shown to be effective in healing ulcers by increasing the mucosal defence mechanisms. Efficacy was assessed by scoring the intensity of day and night pain before, after 2 and after 6 weeks of treatment, and by endoscopy before and after. Tolerance was assessed by routine laboratory tests, physical examination and a survey of any accessory symptoms. Both drugs significantly relieved pain almost at the same rate and to the same extent, whereas endoscopy showed a not significantly greater improvement in the ranitidine group. It was found, however, that the patients in the triletide group had, on average, a significantly greater intensity of intractable factors on entry than those in the ranitidine group (+75%; p less than 0.02). After stratifying the intractability factor intensity, the 5 patients in the triletide sub-group comparable with those in the ranitidine group exhibited exactly the same behavior on pain relief and a very similar one on endoscopy findings (2 healed, 2 improved and 1 unchanged, compared with 7 healed and 3 improved, respectively). The sub-group with greater severity also showed improvements, both symptomatic and endoscopic, but to a lesser extent, indicating the need for prolonged treatment. Tolerance was good with both drugs. Two patients on triletide reported adverse effects; 1 of increased intensity of previous constipation and the other 1 of mild headache and dizziness, but these could not be related definitely to treatment
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| 650 |
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4 |
|a Clinical Trial
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| 650 |
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4 |
|a Comparative Study
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| 650 |
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4 |
|a Journal Article
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| 650 |
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4 |
|a Randomized Controlled Trial
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| 650 |
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7 |
|a Anti-Ulcer Agents
|2 NLM
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| 650 |
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7 |
|a Oligopeptides
|2 NLM
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| 650 |
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7 |
|a triletide
|2 NLM
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| 650 |
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7 |
|a 50Q6LI773L
|2 NLM
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| 650 |
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7 |
|a Ranitidine
|2 NLM
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| 650 |
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7 |
|a 884KT10YB7
|2 NLM
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| 700 |
1 |
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|a Solmi, L
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t 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)
|d 1995
|g 4(1985), 3 Spec No vom: 15., Seite 182-8
|w (DE-627)NLM023961570
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| 773 |
1 |
8 |
|g volume:4
|g year:1985
|g number:3 Spec No
|g day:15
|g pages:182-8
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| 912 |
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| 951 |
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|a AR
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| 952 |
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|d 4
|j 1985
|e 3 Spec No
|b 15
|h 182-8
|