The Efficacy of Cholesterol-lowering Probiotic Lactobacillus Plantarum LPLDL® in Hypercholesterolemic Adults.

NACompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

February 1, 2020

Primary Completion Date

January 1, 2021

Study Completion Date

April 1, 2021

Conditions
Hypercholesterolemia
Interventions
DIETARY_SUPPLEMENT

Lactobacillus plantarum ECGC 13110402

The study will consist of two phases: a treatment period (12 weeks) with either the active or placebo and a wash-out period (4 weeks). Following a screening visit to ensure adherence to the inclusion criteria, the study will consist of a baseline, midpoint, endpoint (week 6 and 12, respectively) and washout visit (week 16).

DIETARY_SUPPLEMENT

Placebo Comparator: Maltodextrin

Please see intervention description above.

Trial Locations (1)

SW15 4JD

Health Sciences Research Centre, Life Sciences Department, University of Roehampton, London

All Listed Sponsors
lead

University of Roehampton

OTHER

NCT03540108 - The Efficacy of Cholesterol-lowering Probiotic Lactobacillus Plantarum LPLDL® in Hypercholesterolemic Adults. | Biotech Hunter | Biotech Hunter