100
Participants
Start Date
October 10, 2021
Primary Completion Date
December 30, 2022
Study Completion Date
May 18, 2023
Sulforaphane, administered as Broccoli sprout extract
Patients will randomized to BSE or Control Group. The group BSE will receive the sulforaphane, administered as broccoli sprout extract for 12 weeks. The dose will increase every four weeks if no side-effects are reported (50 µmmol/day; 100 µmmol/day and 150 µmmol/day, respectivelly). The Control group will receive a placebo (maltodextrin sprayed with copper-chlorophyllin) for the same period (12 weeks). The BSE/placebo will be administered as powder provided in 10 ml of water in the morning in a double-blind manner as dry mixtures in sealed portion size bags of similar shape and size.
Karolinska Institutet, Stockholm
Danderyds sjukhus AB, Stockholm
Skånes universitetssjukhus, Malmo
Skånes University Hospital Sus, Lund
Sahlgrenska Universitetssjukhuset, Gothenburg
Hallands Hospital Varberg, Varberg
Linköpings universitet, Linköping
Västervikssjukhus, Västervik
Västmanlands Hospital Västerås, Västerås
Akademiska sjukhuset, Uppsala
Gävle Hospital, Gävle
Norrlands Universitetssjukhus, Umeå
Lantmännen
UNKNOWN
Karolinska Institutet
OTHER