Yeoh 1993
Supportive Therapie · Version 2.1
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Referenz (Autor, Jahr, Journal) |
Studientyp Mono- vs. Multizentrisch, Verblindung, Randomisierung, Arme, Fallzahl n, Land, Zeitraum |
Patientenmerkmale Indikation, Alter, Geschlecht (m/w), CTX |
Intervention |
Kontrolle |
Zielgröße |
Primary Endpoint |
Secondary Endpoint |
Finanzierung |
Evidenzstufe (CEBM levels/ SIGN) Bei Abwertung: Angabe von Gründen |
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Yeoh 1993 Gut |
Monocenter, double-blind, randomized study, cross-over Two arms + 1 external control N= 18 Australia |
Carcinoma of the genitourinary tract 73 (42-90) yrs. m/f
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N= 18 3 mg Loperamide-N-oxide orally, 2x daily Treatment-Plan: 14 days Loperamide 14 days washout phase 14 days Placebo |
N= 18 3 mg Placebo orally, twice daily |
Gastrointestinal symptoms Absorption of bile acid, vitamin B12, lactose and fat Gastric emptying, gut transit time, intestinal permeability |
Bowel actions/week (13.5 [6-39] vs. 19 [9-53]) Stool frequency/3 days (5 [1-10] vs. 7 [2-14]) (5.25±2.6 vs. 7.5±3.5) Stool weight (260 g [63-1170 g] vs. 450 g [186-1275 g]) |
No information |
National Health and Medical Research Council of Australia Janssen Pharmaceutica |
2b small sample size “…loperamide-N-oxide slows small intestinal transit, increases bile acid absorption, and is effective in the treatment of diarrhea associated with chronic radiation enteritis.” |