CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 233 enrolled
Drug / intervention
Probio-Tec® BG-VCap-6.5 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02819960
NCT02819960Phase 3Completed

Prevention of Irinotecan Induced Diarrhea by Probiotics: A Phase III Study

S&D Pharma SK s.r.o.·interventional·Posted Jun 30, 2016·Updated Dec 14, 2022

In Brief

A Phase 3 clinical trial evaluating Probio-Tec® BG-VCap-6.5 and Placebo for Diarrhea and Cancer. Completed, enrolled 233 participants across 1 site.

Detailed Summary

Diarrhea is a relatively common complication in patients with cancer. At its inception, several mechanisms participated; malabsorption on the basis of mucositis induced by chemotherapy, dysbiosis induced by broad-spectrum antibiotics and predisposition to infectious diarrhea in immunocompromised patients. Some cytostatics and their metabolites can also induce diarrhea directly due to effect on the intestinal mucosa. Use of probiotics in prevention and treatment of diarrhea relies on both the theoretical assumptions and the results of several clinical trials. Lactic acid bacteria involved in the treatment of dysbiosis, compete for substrate with pathogenic bacteria, produce bacterio-cins, increase transepithelial resistance. Their enzymatic activity affects activation or deactivation of metabolites which cause diarrhea. Production of short chain fatty acids, which are important for the maintenance of intestinal mucosal cells also contributes to their antidiarrhoeal effect. This randomized, double-blind, placebo controlled, multicentre trial was designed to evaluate potential of probiotics to prevent grade 3-4 diarrhea in patients treated by irinotecan based chemotherapy during first 6 weeks of irinotecan based chemotherapy

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDiarrhea, Cancer
CountriesSlovakia

Timeline

Phase 3CompletedFinished
20162017201820192020202120222023202420252026
First PostedJun 30, 2016
Enrollment StartMar 1, 2016
Primary CompletionAug 1, 2022
Study CompletionNov 1, 2022
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 10.0 years ago

Interventions

Probio-Tec® BG-VCap-6.5drug

Each capsule contents: 2 lyophilized probiotic strains, total amount of minimum 2,7x10 9 CFU/cps, ratio LGG®: BB-12® = 50% : 50% (Culture percentages are based on cell concentration and are approximate) Lactobacillus rhamnosus GG® (ATCC 53103) Bifidobacterium animalis subsp. lactis BB-12® (DSM 15954) Additives: maltodextrin, microcrystalline cellulose, silicium dioxide, magnesium stearate

Placebodrug

Maltodextrin