Natreon Healthy Skin Study - PrimaVie Supplement

Completed · Phase 1 · Has a placebo group

Conditions studied: Healthy

In brief

This study will demonstrate the ability of the oral supplement, PrimaVie® to improve skin microperfusion, hydration, elasticity and barrier function. 45 females will be enrolled in 1 of 3 arms where they will receive either 125 mg PrimaVie, 250 mg PrimaVie or placebo (control) to take twice daily for 14 weeks.

Key facts

Study ID
NCT02762032
Run by
Ohio State University
People needed
45
Starts
2016-02-20
Expected to finish
2019-12-20
Last updated by the study team
2026-06-25

Who can join

Age: 30 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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