RecruitingNCT07367126

Neuropathic Pain in Knee Osteoarthritis: Pain Severity and Functional Status

Presence of Neuropathic Pain in Knee Osteoarthritis: Relationship Between Pain Severity and Functional Status


Sponsor

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Enrollment

102 participants

Start Date

Dec 20, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

Osteoarthritis (OA) is a degenerative joint disease characterized by structural changes such as cartilage loss and osteophyte formation, leading to functional limitations and disability. Pain in knee OA involves a complex pathophysiological structure including both nociceptive and neuropathic mechanisms. Identifying the neuropathic pain component is clinically significant for improving quality of life and functional recovery. This cross-sectional controlled clinical study aims to determine the prevalence of neuropathic pain in patients with knee OA and evaluate its impact on pain severity and functional status. Patients will be categorized based on the Douleur Neuropathique 4 (DN4) questionnaire and assessed using various pain and functional scales.


Eligibility

Min Age: 40 YearsMax Age: 70 Years

Inclusion Criteria3

  • Diagnosed with Knee OA according to ACR criteria.
  • Knee pain for more than 3 months.
  • Voluntary participation.

Exclusion Criteria10

  • History of surgical intervention in the affected knee.
  • History of trauma to the affected knee within the last 6 months.
  • History of intra-articular injections (e.g., corticosteroids, hyaluronic acid, PRP) or physical therapy involving the affected knee within the last 6 months.
  • Presence of severe psychiatric disorders such as severe depression, anxiety disorder, or psychosis.
  • Diagnosis of central nervous system diseases, including Parkinson's disease or multiple sclerosis.
  • Diagnosis of inflammatory arthritis, such as Rheumatoid Arthritis or Ankylosing Spondylitis.
  • Severe cognitive impairment.
  • Chronic decompensated cardiac, renal, or hepatic failure.
  • Severe psychiatric, neurological, or kognitive disorders.
  • Decompensated cardiac, renal, or hepatic failure.

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Interventions

OTHERClinical and Functional Assessment

All participants will undergo a one-time, cross-sectional clinical assessment. Comprehensive demographic and clinical data, including age, body mass index (BMI), educational level, occupation, and marital status, will be recorded for each participant. Pain intensity will be measured using a 10-cm Visual Analog Scale (VAS). Functional status and symptoms related to knee osteoarthritis will be evaluated using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the Knee Injury and Osteoarthritis Outcome Score-Physical Function Short Form (KOOS-PS). To ensure consistency and minimize measurement error, all anthropometric measurements, specifically weight and height, will be performed by the same researcher.


Locations(1)

Istanbul Physical Medicine and Rehabilitation Training and Research Hospital

Istanbul, Turkey (Türkiye)

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NCT07367126


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