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Study identifier: NCT07488936 Synced from ClinicalTrials.gov · July 29, 2026
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Effects of Low Back Pain Types on Pain Severity and Quality of Life in Patients With Failed Back Surgery Syndrome

Condition: Failed Back Surgery Syndrome · Chronic Pain  ·  Sponsor: Konya Beyhekim Training and Research Hospital

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of this study is to determine the effects of different types of low back pain on pain intensity and quality of life in patients with failed low back surgery syndrome. The study will include 200 patients with failed lumbar spine surgery syndrome who present to the physical therapy and rehabilitation (FTR) outpatient clinics of Konya Beyhekim Training and Research Hospital with complaints of lower back pain lasting at least 3 months. Patients will be evaluated in a single session. The Visual Analog Scale (VAS), Pain Catastrophizing Scale (PCS) will be used to determine the patients' pain level and impact, the Roland-Morris Disability Questionnaire (RMDQ) will be used for functionality assessment, and the SF-36 score will be used for quality of life assessment. To determine the type of pain: Those with pain levels above the cutoff value on the DN4 (Douleur Neuropathique 4 Questions) pain scale will be diagnosed with neuropathic pain. For nociplastic pain affecting the musculoskeletal system, a diagnosis of nociplastic pain will be made according to clinical criteria and grading scores. Those who do not meet these criteria will be classified as having nociceptive pain.

This description comes directly from the study's public registry record.

Talk to the study team

emrah çetin, doctor  ·  +905417606950  ·  dremrahcetin4547@gmail.com

SAVAŞ KARPUZ, AASSOCIATE PROFESSOR DOCTOR  ·  +905552057860  ·  svskrpz@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Konya Beyhekim Eğitim Araştırma HastanesiKonya, Selçuklu, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07488936