The Effect of Micro Fragmented Adipose Tissue (MFAT) on Shoulder Osteoarthritis

Description

This is a non-surgical trial comparing the clinical and functional outcomes of patients with osteoarthritis treated with Intra-articular injection of Micro Fragmented Adipose Tissue versus conventional therapy of intra-articular injection of corticosteroid.

Conditions

Osteoarthritis Shoulder, Shoulder Pain

Study Overview

Study Details

Study overview

This is a non-surgical trial comparing the clinical and functional outcomes of patients with osteoarthritis treated with Intra-articular injection of Micro Fragmented Adipose Tissue versus conventional therapy of intra-articular injection of corticosteroid.

The Effect of Micro Fragmented Adipose Tissue (MFAT) on Shoulder Osteoarthritis

The Effect of Micro Fragmented Adipose Tissue (MFAT) on Shoulder Osteoarthritis

Condition
Osteoarthritis Shoulder
Intervention / Treatment

-

Contacts and Locations

Stanford

Stanford University, Stanford, California, United States, 94305

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

  • * Age between 25 and 75 years-old
  • * Diagnosis of pre-existing osteoarthritis of the glenohumeral joint
  • * Working understanding of the English language and able to fully understand the procedure
  • * Capable of providing informed consent
  • * Able to complete online, in-person or phone surveys for the purposes of follow-up
  • * Capable of understanding pre- and post-procedure care instructions
  • * Ambulatory at baseline
  • * Previous trial and failure of conservative therapy consisting of a minimum of 6 weeks of physical therapy and trial of anti-inflammatory medications if not contraindicated, with or without concomitant bracing and/or injections.
  • * Age \< 25 or \> 75 years old
  • * Radiographs demonstrating either no, little osteoarthritis, severe(bone on bone) osteoarthritis
  • * Prior total or partial joint replacement surgery or surgery involving cartilage regeneration
  • * Previous cortisone, PRP or Hyaluronic acid intra-articular injection within the last 3 months
  • * Co-morbidity with the rheumatologic condition, inflammatory arthritis
  • * Currently undergoing immunomodulatory therapy
  • * Uncontrolled endocrine disorder
  • * BMI \>40 or joint space not visible by ultrasound
  • * Current diagnosis of osteomyelitis, human immunodeficiency virus (HIV-1, -2) and/or hepatitis C (HCV), infection, and poorly controlled diabetes (HgA1C \>7.0)
  • * Pregnancy or planned pregnancy
  • * previous stem cell injection into treatment joint
  • * Patient scheduled to undergo any concomitant shoulder surgical procedures or other surgery which may affect outcomes.
  • * Coagulopathy or anticoagulant treatment
  • * Chronic pain involving multiple body parts or opioid medication management
  • * Diagnosis of fibromyalgia
  • * Concomitant massive(2 tendons with retraction), complete rotator cuff tendon tear

Ages Eligible for Study

25 Years to 75 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Stanford University,

Study Record Dates

2025-12-31