Clinical Trial Details

Trial ID: L0933
Source ID: ISRCTN05474560
Associated Drug: VSL#3
Title: The impact of VSL#3 probiotic on cardiovascular risk and liver injury in patients with non alcoholic fatty liver disease: a randomised, double blinded, placebo controlled proof-of-concept trial
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Diabetes Research Network, Oral and Gastrointestinal <br>Not Applicable
Interventions: Two study visits per participant, randomised to receive either treatment or placebo on a 1:1 ratio. Treatment arm will take VSL#3 probiotic 2 sachets twice a day for 10 weeks. Placebo arm will take placebo 2 sachets twice a day for 10 weeks. Participants
Outcome Measures: Cardiovascular biomarkers pre and post interventionLiver fat and inflammation - compare fibrosis risk score and structural liver changes before and after study intervention
Sponsor/Collaborators: Portsmouth Hospitals NHS Trust (UK)
Gender: All
Age: nannan
Phases: Not applicable
Enrollment: 60
Study Type: Interventional
Study Designs: Randomised interventional trial (Treatment)
Start Date: 09/08/2012
Completion Date: --
Results First Posted: --
Last Update Posted: 17 October 2016
Locations: United Kingdom
URL: http://isrctn.com/ISRCTN05474560