Clinical Trials Directory

Trials / Suspended

SuspendedNCT01477866

Utility Of Citogenex Administration In Patients With Colon-Rectal Cancer

Status
Suspended
Phase
N/A
Study type
Interventional
Enrollment
250 (estimated)
Sponsor
University of Palermo · Academic / Other
Sex
All
Age
40 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The main aim of the present study is to test the efficacy and safety of CITOGENEX administration in patients with colon-rectal cancer.

Detailed description

CITOGENEX is a dietary supplement of insoluble polysaccharides, of Lactobacillus Casei (specific type) and of Bifidobacterium Lactis (specific type). These subspecies of probiotics bacteria have been shown to be effective in improving the immunity. Several trials are currently underway, in order to evaluate the effects of probiotics as potential novel therapies in addition to traditional therapeutic approaches. Although probiotics do not play an anti-tumor action per se, these agents may significantly contribute to decrease the typical side effects due to traditional anti-tumor treatments, such as gastrointestinal symptoms, immunity deficit, as well as the alterations in the gut lymphoid tissue. It is therefore expected that CITOGENEX may have several significant beneficial effects in patients under anti-tumor treatments. In order to test this hypothesis, we will perform a randomized, single-blind, two-arms, prospective study in patients with colon-rectal cancer.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTcitogenexCITOGENEX is a dietary supplement of insoluble polysaccharides, of Lactobacillus Casei (specific type) and of Bifidobacterium Lactis (specific type).
OTHERconventional therapyconventional therapy for colon-rectal cancer

Timeline

First posted
2011-11-23
Last updated
2017-12-12

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01477866. Inclusion in this directory is not an endorsement.