This study will assess the safety and efficacy of zoledronic acid in patients presenting with spontaneous osteonecrosis of the knee.
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Proof of Concept Study of Zoledronic Acid in Spontaneous Osteonecrosis of the Knee (SONK)
Conditions
Osteonecrosis
Study Type
Interventional
Study Design
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Further Details
Primary Outcome Measures:
- Changes from baseline after 3 months in a) knee pain scores (using the KOOS pain subscale), and b) volume of osteonecrotic lesion (indicated by bone marrow oedema) on MRI. [Time Frame: 3 months]
Secondary Outcome Measures:
- Changes from baseline after 6 months in a) knee pain scores (using the KOOS pain subscale), and b) volume of osteonecrotic lesion (indicated by bone marrow oedema) on MRI. [Time Frame: 6 months]
- Safety as assessed by adverse events.
Study Start
May 2007
Eligibility & Criteria
- Ages Eligible for Study: 40 Years – 85 Years
- Genders Eligible for Study: Both
Inclusion Criteria:
- Adults 40-85 years of age
- Diagnosis of painful osteonecrosis of the knee within the last month.
Exclusion Criteria:
- Intravenous (iv) bisphosphonates within the last 2 years.
- Abnormal thyroid, kidney or liver function.
- Abnormal blood calcium or alkaline phosphatase levels.
Other protocol-defined inclusion/exclusion criteria may apply
Total Enrolment
20
Contact Details
- Novartis Investigative Site, Gordon, NSW,2072, Australia
Contact Novartis Australia
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