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NSAID Treatment in Knee Osteoarthritis

Phase 4
Completed
Conditions
Knee Osteoarthritis
Interventions
Registration Number
NCT01860833
Lead Sponsor
University of Catanzaro
Brief Summary

Central mechanisms may play a role in pain perception during osteoarthritis (OA).Local inflammation (which involves production of pro-inflammatory cytokines such as interleukin (IL) 4 TNF-alpha, IL-6 and IL-8) is considered to be a major source of pain.

Certain therapies that specifically interfere with the expression or actions of pro-inflammatory cytokines have been explored. NSAIDs have analgesic, antipyretic and anti-inflammatory properties and are extensively prescribed for several musculoskeletal disorders. Indeed, the Osteoarthritis Research Society International (OARSI) recently recommended the use of NSAIDs for management of knee and hip OA in symptomatic patients. These drugs have been shown to influence cytokine metabolism in the synovial fluid of OA patients with satisfactory relief of painful osteoarthritic joints.

The aim of the current study was to explore whether NSAID treatment inhibits TNF-alpha, IL-6, IL-8, and VEGF secretion in the synovial fluid of osteoarthritic joints. In particular, diclofenac, ibuprofen and celecoxib were studied. Under the hypothesis that relationships between proinflammatory cytokines and the clinical status of OA patients are possible, we also evaluated the association between the concentration of these molecules in the osteoarthritic knee synovial fluid and the pain and functional status of patients with OA. The effects of NSAIDS on signal transduction pathways in the synovial membrane were also investigated.

Detailed Description

not desired

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
Inclusion Criteria

Patients eligible for the study were:

  • older than 50 years and
  • had primary knee OA diagnosed according to the clinical and radiological criteria of the American Rheumatism Association.

Further inclusion criteria were:

  • clinical signs of joint inflammation (warmth, swelling or effusion) and
  • a disease severity grade 2 or 3 according to the Kellgren-Lawrence classification
Exclusion Criteria
  • allergy to NSAIDs,
  • progressive serious medical conditions (such as cancer, AIDS or end-stage renal disease),
  • history of gastrointestinal ulcer or bleeding,
  • a hemoglobin concentration lower than 11.5 g/dL,
  • renal diseases (serum creatinine concentration more than 1.2 times the upper limit of the normal range according to the central laboratory definition reference values), or
  • liver dysfunction (serum alanine or aspartate transaminase concentrations more than 1.5 times the upper limit of normal range according to the central laboratory definition reference values).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
celecoxib 200 mg/dayCelecoxibcelecoxib 200 mg once day
ibuprofen 1200 mg/dayIbuprofenibuprofen 600 mg bid
diclofenac 75 mg/dayDiclofenacdiclofenac 75 mg once day slow release
diclofenac 150 mg/dayDiclofenacdiclofenac 75 mg bid
ibuprofen 1800 mg/dayIbuprofenibuprofen 600 mg tid
celecoxib 400 mg/dayCelecoxibcelecoxib 200 mg bid
Primary Outcome Measures
NameTimeMethod
Western Ontario and McMaster universities (WOMAC) osteoarthritis index score0-14 days

Womac was used to 77 measure the disease-specific health status of patients before and after the pharmacological treatment.

Secondary Outcome Measures
NameTimeMethod
Naranjo probability scale14 days

The Naranjo probability scale was used to evaluate the development of adverse drug reaction during this study

Trial Locations

Locations (1)

Department of Orthopedic and Trauma Surgery

🇮🇹

Catanzaro, Italy

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