Safety & Effectiveness of Autologous Regenerative Cell Therapy on Pain & Inflammation of Osteoarthritis of the Shoulder

Description

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 shoulder. Follow-up will consist of a larger sample including 4,000 patients.

Conditions

Osteoarthritis

Study Overview

Study Details

Study overview

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 shoulder. Follow-up will consist of a larger sample including 4,000 patients.

Safety and Effectiveness of Autologous Regenerative Cell Therapy on Pain and Inflammation Associated With Osteoarthritis of the Shoulder

Safety & Effectiveness of Autologous Regenerative Cell Therapy on Pain & Inflammation of Osteoarthritis of the Shoulder

Condition
Osteoarthritis
Intervention / Treatment

-

Contacts and Locations

Grove City

VivaTech International, Inc., Grove City, Pennsylvania, United States, 16127

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patients with indication of Osteoarthritis. 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 shoulder pain with the index side (left or right shoulder).
  • 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, 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. Treatments with strong opioid drugs in the previous 4 weeks for other pain rather than shoulder osteoarthritis
  • 2. Corticosteroid injection at treatment site within 1 month
  • 3. Consistent use of NSAIDs within 48 hours of procedure.

Ages Eligible for Study

18 Years to 90 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

VivaTech International, Inc.,

Mark LoDico, MD, PRINCIPAL_INVESTIGATOR, Advanced Regenerative Medicine

Study Record Dates

2025-08