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Clinical Trial Summary

To evaluate the effect and support the tolerance of orally ingested formulation containing Eurycoma longifolia dietary supplement (Euryco-10) on a cohort of senior men.


Clinical Trial Description

This is a single-center, single arm, open label study in senior men. This study will investigate the effect and tolerance of oral ingestion of Euryco-10. Subjects meeting all inclusion and none of the exclusion criteria will be enrolled and provided with study dietary supplement. Subjects will be instructed to take 2 capsules per day for 35 days. Administration and any adverse events will be recorded in the subject diary. At each clinic visit (Day 0, Day 21 and Day 35) the Subject will complete the AMS Questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04584918
Study type Observational
Source Innovus Pharmaceuticals, Inc.
Contact
Status Not yet recruiting
Phase
Start date October 2020
Completion date January 2021

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