Recruiting
Phase 2

Autologous Cell Therapy

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

Study Details

Brief summary:

This is a prospective open-label clinical study of 50 patients to determine safety and treatment potential of autologous cell therapy for pain and inflammation associated with Osteoarthritis of the knee. Follow-up will consist of a larger sample including 4,000 patients.

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

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Patients with indication of Osteoarthritis, grade 2 or more. Can be from degeneration or chronic injury.
2. Patients range from 18-90 years of age.
3. Patients must be able to comply with treatment plan, laboratory tests and periodic interviews.
4. Patients with adequate renal function, Creatinine ≤ 1.5 mg/dl.
5. Patients with adequate cardiac and respiratory function.
6. Patients with adequate blood coagulation activity, PT(INR) < 1.5, APTT
7. Patients must have adequate immune system function, with no known immunodeficiency disease.
8. Greater than 6 months knee pain on the index side (left or right knee).

Exclusion Criteria:

1. Neoplastic cancer within 5 years prior to screening, except for cutaneous basal cell or squamous cell cancer resolved by excision
2. Presence of clinically significant acute or unstable cardiovascular and cerebrovascular (stroke).
3. Diagnosis of a transient ischemic attack in the 6 months prior to screening.
4. Patients infected with hepatitis B, C or HIV.
5. Patients with Body Mass Index (BMI) > 40kg/m2
6. Presence of active infection.
7. Any other illness, psychiatric disorder, alcohol or chemical dependence that in the opinion of the investigator would render a patient unsuitable to participate in the study.
8. Conditions/therapies/factors which could confound or interfere with the evaluation of pain/mobility including, but not limited to:

1. Knee instability.
2. A varus/valgus deformity of more than 10o, a deformity requiring osteotomy or complex surgery.
3. Gout or pseudo gout
4. Treatments with strong opioid drugs in the previous 4 weeks for other pain rather than knee osteoarthritis
5. Corticosteroid injection at treatment site within 1 month
6. Consistent use of NSAIDs within 48 hours of procedure.

Study Design

Enrollment

4000 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Cohort 1

Interventions assigned by Principal Investigator

experimental: Cohort 2

Interventions assigned by Principal Investigator

Interventions

[StroMed + platelet rich plasma (PRP)]

\[Day 0\] - Because no enzymes or drugs are added with this mechanical process, the resulting cell concentrate still contains the extra-cellular matrix. In addition, the cells have not been altered by manipulation with enzymes or culturing. This autologous, cell concentrate is of minimal risk to the patient with no artificial ingredients added. Also Platelet Rich Plasma processed by the RegenLab (RegenKit BCT-3) PRP product and by direct injection to the affected joint.

[PRP] platelet rich plasma

Additional treatments with Platelet Rich Plasma processed by the RegenLab (RegenKit BCT-3) PRP product and by direct injection to the affected joint. Days 7,14 and 30

[PRP] platelet rich plasma

Additional treatments with Platelet Rich Plasma processed by the RegenLab (RegenKit BCT-3) PRP product and by direct injection to the affected joint. Days 30 and 60

Primary outcome measure

  • Change is being assessed for the KOOS survey (Knee Osteoarthritis Outcome Score) [ Time Frame: 0, 2, 6 months ]

Central Contacts and Locations

Central contacts

Locations

VivaTech International, Inc.

Recruiting

Grove City, Pennsylvania, United States, 16127

Contacts

Principal Investigator:

Mark LoDico, MD

More Information

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.