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Completed

NCT Number: NCT03125499

A Prospective Observational Study to Evaluate Long-term Changes in Cartilage Morphology in Subjects Who Previously Received TPX-100 or Placebo in Study TPX-100-1 for Patellar Osteoarthritis Involving Both Knees

To evaluate the long-term changes in patellar cartilage thickness in TPX-100 versus placebo-treated knees in subjects who participated in Study TPX-100-1 or TPX-100-2.

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Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Dr. Samy Metyas

Covina, California, 91722, United States

About this study

No drug intervention. Study to collect 1 additional MRI of each knee treated in either TPX-100-1 or TPX-100-2.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects who participated in TPX-100-1 and received 4 injections of 200 mg/injection TPX-100 in one knee, or subjects who participated in TPX-100
  • Cruciate and collateral ligament stability as assessed by screening history and clinical examination
  • Stable medial and lateral menisci as assessed by screening history and clinical examination
  • Able to read, understand, sign and date the subject informed consent

Exclusion criteria

  • Contraindication to MRI, including: metallic fragments, clips or devices in the brain, eye, or spinal canal; implanted devices that are magnetically programmed; weight > 300 lbs.; moderate or severe claustrophobia; previous intolerance of MRI procedure
  • Prior surgery in the knees, excluding procedures for debridement only (no previous microfracture procedure)
  • History of rheumatoid arthritis, psoriatic arthritis, or any other autoimmune or infectious cause for arthritis
  • Last viscosupplementation (e.g. Synvisc® or similar hyaluronic acid product) injected into either knee < 3 months before enrollment
  • Last intra-articular knee injection of corticosteroids < 3 months before enrollment
  • Use of any steroids (except inhaled corticosteroids for allergy or respiratory problems) during the previous month before enrollment
  • History of arthroscopy in either knee in the 3 months before enrollment
  • History of septic arthritis, gout or pseudo-gout in either knee in the 12 months before enrollment
  • Clinical signs of acute meniscal tear (locking, new acute mechanical symptoms consistent with meniscal tear)
  • Active systemic infection
  • Participation in other clinical osteoarthritis drug studies, except for studies TPX-100-1 and TPX-100-2, within two years prior to enrollment in TPX-100-4.

Treatment and study plan

Previous treated with TPX-100

Other

No intervention, only observational

Other names: AC-100

Primary outcomes

  1. Evaluate the long-term changes in patellar cartilage thickness

    Time frame: Between 24 and 34 months from initial drug treatment

    Quantitative analysis of long-term changes in patellar cartilage thickness by MRI

Secondary outcomes

  1. Examine intra-subject longitudinal changes in patellar cartilage volume between TPX-100 versus placebo-treated knees by MRI

    Time frame: Between 24 and 34 months from initial drug treatment

    Examine intra-subject longitudinal changes in patellar cartilage volume between TPX-100 versus placebo-treated knees by MRI

  2. Examine intra-subject longitudinal changes in thickness and thinness scores of cartilage in the central (non-patellar) compartment of knees

    Time frame: Between 24 and 34 months from initial drug treatment

    Examine intra-subject longitudinal changes in thickness and thinness scores of cartilage in the central (non-patellar) compartment of knees

  3. Examine intra-subject longitudinal changes in Patient reported outcome measures

    Time frame: Between 24 and 34 months from initial drug treatment

    Examine intra-subject longitudinal changes in Patient Reported Outcome Measures

Sponsors and collaborators

Lead sponsor

OrthoTrophix, Inc

Industry

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2018
First posted
Apr 24, 2017
Registry last updated
Apr 5, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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