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

Osteoarthritis Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02844738
• Other study ID #: ? IRCM-2016-113
• Status: Recruiting
• Phase: Phase 2
• Start date: July 2015
• Est. completion date: August 2025

Study information

• Verified date: August 2023
• Source: VivaTech International, Inc.
• Contact: Scott M Herkes, MBA
• Phone: 855-984-8287
• Email: scott.herkes[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

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

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.

Patients will be treated for Osteoarthritis (OA) of the shoulder due to degeneration or chronic injury. They will be treated with autologous Stromed obtained by the Adipose Ultrasonic Cell Recovery Unit (AUCRU) and Platelet Rich Plasma (PRP) processed by the RegenLab (RegenKit BCT-3) PRP product each as direct injections to the affected joints. Patient outcomes will be tracked with laboratory tests for inflammation markers, the DASH and SPADI questionnaires and a follow up MRI at various endpoints to 6 months. SF-36 forms (a quality of life measure) and numerical ratings scales (NRS) will also be used to assess safety and efficacy of treatment, as well as any reduction in patient medication and/or delay in pending shoulder planning/replacement therapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 4000
• Est. completion date: August 2025
• Est. primary completion date: August 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion 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).

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, 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.

Related Conditions & MeSH terms

• Inflammation
• Osteoarthritis

Intervention

Biological:
• [StroMed + platelet rich plasma (PRP)]
Patients will be treated with autologous StroMed obtained by the Adipose Ultrasonic Cell Recovery Unit and Platelet Rich Plasma processed by the RegenLab (RegenKit BCT-3) PRP product each as direct injections to the affected joints at the time of initial treatment. Thereafter the affected joints will be treated as direct injections to the joint with Platelet Rich Plasma processed by the RegenLab (RegenKit BCT-3) PRP product. Day 0 [StroMed + platelet rich plasma (PRP)], Days 7 and 14 [PRP]

Locations

Country	Name	City	State
United States	VivaTech International, Inc.	Grove City	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
VivaTech International, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change is being assessed for the DASH Survey (Disabilities of the Arm, Shoulder, Hand	Disabilities of the Arm, Shoulder, and Hand	0,2,6 months
Secondary	Change is being assessed by MRI of afflicted joint	Looking for cartilage regrowth via MRI	0 and (6 months optional)
Secondary	Change is being assessed for the SPADI Survey (Shoulder Pain and Disability Index)	Shoulder Pain and Disability Index	0,2,6 Months
Secondary	Change is being assessed for the SF36 Survey (Short Form Health Survey)	Short Form Health Survey	0,2,6 Months
Secondary	Change is being assessed for the NRS Survey (Numerical Rating Scale for Pain)	Numerical Rating Scale for Pain	0,2,6 Months

External Links

•   Company Website