Overview
Viscosupplementation in the Hip Following Hip Arthroscopy
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
Hip arthroscopy is a rapidly evolving procedure that has seen an exponential increase in the number of cases performed yearly. With hip arthroscopy still in its infancy in relation to knee and shoulder arthroscopy, there are still many questions yet to be answered. Axioms that were once thought to be true regarding indications and treatment for hip arthroscopy are continually being revised. As with the knee and shoulder before it, the hip is now graduating into treatment avenues that were otherwise thought to only be possible through an open surgical procedure. Viscosupplementation in patients post arthroscopy with known articular cartilage injury has been shown to be efficacious. The pathophysiology of hyaline degradation during the arthritic process within the knee has been studied, and with this understanding has grown the widespread usage of viscosupplementation. While questions still exist regarding the effectiveness of viscosupplementation in non-weightbearing joints, it appears the benefits seen in the weight bearing joints, such as the knee, are apparentPhase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Rothman Institute OrthopaedicsCollaborator:
Sean McMillan, DOTreatments:
Hyaluronic Acid
Criteria
Inclusion Criteria:Preoperative inclusion criteria will be made via x-ray and MRI evaluation. These criteria
shall include: 2 mm or greater joint space preservation of the hip on radiographs, absence
of acetabular subcortical bone cysts, Tonnis Score less than 2 on radiographs, and patient
age greater than 18.4 Intra-operative evaluation of the cartilage will be performed by the
surgeon on both the acetabular and femoral head sides. Patients shall be included if the
osteochondral defect meets Outerbridge Classification criteria of stage II or greater.
Furthermore the lesion shall be greater than 1cm in size (and thus not amenable to other
procedures such as microfracture). Subjects must be willing to sign the IRB-approved
informed consent and be older than 18 years old.
Exclusion Criteria:
All patients 55 years of age and older. All patients with previous hip surgery on a
concomitant side. Patients who present a history of radiculopathy or regional pain
syndrome. Patients with a worker's compensation claim or pending litigation claim. Patients
with Outerbridge Grade IV changes on either acetabular or femoral articular cartilage.