Status and phase
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About
Primary: To determine factors that affect absorption and serum levels of lycopene after supplementation.
Secondary:
Full description
This is an uncontrolled intervention study in which eligible male subjects (N=60), after a two-week washout, will be randomized to receive lycopene either 15 or 30 mg per day for 12 weeks. About equal numbers of subjects will be randomized to either 15 or 30 mg of lycopene (about 30 subjects for each arm). The study is expected to be finished in 2 year. The study is expected to be finished in 2 year. Concerning an expected dropout rate of 10%, 66 subjects will be recruited for the study.
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Interventional model
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74 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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