Salminen 1988
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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Clinical Radiology |
Monocenter Randomized study Two arms N= 24 Finnland |
Cervix and uterus carcinoma 40-75 yrs. female Postoperative radiation therapy |
N= 11 Dietary counselling (fat-free diet, low-residue diet) and 150 ml fermented milk test product 2x109 live Lactobacillus acidophilus bacteria and 6,5% lactulose One per day, 5 days prior to RT, throughout RT and for ten days after finishing the treatment regimen |
N= 10 Dietary counselling (fat-free diet, low-residue diet) |
Incidence of diarrhea at different control times: before treatment (1), during the treatment (2, 3, 4), six weeks after the treatment (5) |
Incidence of diarrhea control time 1 (0/11 vs. 0/10) control time 2 (3/11 vs. 8/10) (p<0.01) control time 3 (2/11 vs. 9/10) (p<0.01) control time 4 (2/11 vs. 8/10) (p<0.01) control time 5 (3/11 vs. 9/10) (p<0.01) Use of antidiarrhoeal drugs (1/11 vs. 6/10) (p<0.01) |
Test Group tolerated the yoghurt treatment well. |
No information |
2b-/1- Small sample size, no blinding, no placebo was given “The results indicated that the test product appeared to prevent radiotherapy-associated diarrhea.” |