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Recruiting NCT07367126

NCT07367126 Neuropathic Pain in Knee Osteoarthritis: Pain Severity and Functional Status

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Clinical Trial Summary
NCT ID NCT07367126
Status Recruiting
Phase
Sponsor Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Condition Knee Osteoarthristis
Study Type OBSERVATIONAL
Enrollment 102 participants
Start Date 2025-12-20
Primary Completion 2026-03-31

Eligibility & Interventions

Sex All sexes
Min Age 40 Years
Max Age 70 Years
Study Type OBSERVATIONAL
Interventions
Clinical and Functional Assessment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 102 participants in total. It began in 2025-12-20 with a primary completion date of 2026-03-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * Diagnosed with Knee OA according to ACR criteria. * Knee pain for more than 3 months. * Voluntary participation. Exclusion Criteria: * 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.

Contact & Investigator

Central Contact

Eser Kalaoglu, M.D.

✉ eserkalaoglu@hotmail.com

📞 +90 (212) 496 50 00

Principal Investigator

Eser Kalaoglu, M.D.

PRINCIPAL INVESTIGATOR

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Frequently Asked Questions

Who can join the NCT07367126 clinical trial?

This trial is open to participants of all sexes, aged 40 Years or older, up to 70 Years, studying Knee Osteoarthristis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07367126 currently recruiting?

Yes, NCT07367126 is actively recruiting participants. Contact the research team at eserkalaoglu@hotmail.com for enrollment information.

Where is the NCT07367126 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07367126 clinical trial?

NCT07367126 is sponsored by Istanbul Physical Medicine Rehabilitation Training and Research Hospital. The principal investigator is Eser Kalaoglu, M.D. at Istanbul Physical Medicine Rehabilitation Training and Research Hospital. The trial plans to enroll 102 participants.

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