Understanding pain and quality of life in patients with cervical radiculopathy
Functional Limitation, Pain, Disability and Quality of Life in Patients With Cervical Spondylotic Radiculopathy
This study looks at how pain and everyday challenges affect the quality of life for people with cervical radiculopathy caused by spinal stenosis.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 64 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Karabuk University Academic / other |
| Locations | 1 site (Karabük) |
| Trial ID | NCT06001359 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the relationship between functional limitations, pain, and quality of life in patients suffering from cervical spondylotic radiculopathy. It focuses on individuals with lateral-foraminal spinal stenosis, assessing symptoms such as pain, numbness, and weakness in the affected limbs. The study will utilize diagnostic imaging techniques like MRI and CT to confirm the diagnosis and gather data on the impact of this condition on daily living. By analyzing these factors, the study seeks to provide insights into the challenges faced by patients and the overall burden of the condition.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old with lateral-foraminal spinal stenosis in the cervical region and associated unilateral root symptoms.
Not a fit: Patients with severe neurological deficits, recent cervical surgery, or other significant spinal conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of cervical radiculopathy, leading to improved management strategies and better quality of life for affected patients.
How similar studies have performed: While there is existing literature on cervical radiculopathy, this specific observational approach focusing on the interplay of pain, function, and quality of life is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * over 18 years of age * with lateral-foraminal spinal stenosis in the cervical region * with or without neck pain consistent with the diagnosis obtained from magnetic resonance imaging * with unilateral root symptoms such as pain, numbness, weakness in the affected limb, and diagnosis based on MRI and computerized tomography Exclusion Criteria: * signs of increased ventral pressure, such as ventral osteophytes, disc calcification, and ligament hypertrophy * severe neurological deficits, pregnant women, spinal malignancies, * those who had undergone cervical surgery in the last 12 months * and those who could not cooperate
Where this trial is running
Karabük
- Karabuk University — Karabük, Turkey (Recruiting)
Study contacts
- Study coordinator: Aydın Sinan Aydın Sinan, +905065897613
- Email: dr.sinanapaydin@yahoo.com
- Phone: +905065897613
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.