Status:

UNKNOWN

Synovial Fluid Biomarkers Pre and Post Hymovis Knee Injection

Lead Sponsor:

National Jewish Health

Collaborating Sponsors:

Fidia Pharma USA Inc.

Conditions:

Knee Osteoarthritis

Eligibility:

All Genders

21-80 years

Brief Summary

This NJH Investigator Initiated Study funded by Fidia will prospectively perform 2 ultrasound (US) guided knee aspirations in patients with knee osteoarthritis using a pneumatic compressive device (Kn...

Detailed Description

50 Subjects between 21-80 years with a BMI \< 40 with mild to moderate knee osteoarthritis on x ray (KL grade II or III) will have a ultrasound guided arthrocentesis with an external pneumatic compres...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Mild to moderate knee osteoarthritis on x ray
  • age 21-80
  • Exclusion Criteria
  • pregnant
  • BMI \> 40
  • history of systemic immune disorders
  • knee arthroplasty with replacement
  • knee infection or surgery within 1 year
  • glucocorticoid injection within 3 months inability to ambulate for 6 minutes without walking assistive devices
  • unable to provide informed consent
  • patients with a clinical contra-indication for an arthrocentesis or adverse reaction to prior intra-articular lidocaine or HA injections.

Exclusion

    Key Trial Info

    Start Date :

    January 1 2019

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    February 1 2022

    Estimated Enrollment :

    50 Patients enrolled

    Trial Details

    Trial ID

    NCT04093232

    Start Date

    January 1 2019

    End Date

    February 1 2022

    Last Update

    March 3 2021

    Active Locations (1)

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    national Jewish health

    Denver, Colorado, United States, 80206