Sponsor:
VivaTech International, Inc.
Code:
NCT02844751
Conditions
Osteoarthritis
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Accepted
Interventions
[StroMed + platelet rich plasma (PRP)]
[PRP] platelet rich plasma
[PRP] platelet rich plasma
Brief summary:
Conditions
Osteoarthritis
Study ID
NCT02844751
Start date
Jul, 2015
Status verified date
Oct, 2025
Completion date
Aug, 2026
Anticipated
Primary completion date
Aug, 2026
Anticipated
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Accepted
Enrollment
4000 participants
Anticipated
Allocation
Non randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
experimental: Cohort 1
experimental: Cohort 2
Interventions
[StroMed + platelet rich plasma (PRP)]
[PRP] platelet rich plasma
[PRP] platelet rich plasma
Primary outcome measure
Central contacts
Locations
VivaTech International, Inc.
Recruiting
Grove City, Pennsylvania, United States, 16127
Contacts
Principal Investigator:
Mark LoDico, MD
Sponsor
VivaTech International, Inc.
Last update posted
Oct 14, 2025
Last verified
Oct, 2025
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by VivaTech International, Inc. on 2025-10-14.