Bandırma Onyedi Eylul University Faculty of Medicine
Balıkesir, Bandırma, 10200, Turkey (Türkiye)
Location contact
Ayşe Güldem Kilciler, Prof.
CONTACT
Nurten Nas Kırdar, Assistant Professor
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07425470
The aim of this study was to epidemiologically evaluate patients diagnosed with spinal cord injury who were admitted to our clinic over the last five years and, unlike similar studies, to investigate the presence of complications in these patients. The investigators hope that this study will contribute to the literature by raising awareness of spinal cord injury epidemiology and potential complications.
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Observational
Balıkesir, Bandırma, 10200, Turkey (Türkiye)
Ayşe Güldem Kilciler, Prof.
CONTACT
Nurten Nas Kırdar, Assistant Professor
PRINCIPAL_INVESTIGATOR
This study was designed as a retrospective descriptive study. Patients who were admitted to the Physical Medicine and Rehabilitation outpatient clinic of Bandırma Training and Research Hospital with a diagnosis of paraplegia or tetraplegia between December 1, 2020, and December 1, 2025, were included in the study. These diagnoses were screened using the following ICD-10 codes: G82 (paraplegia and tetraplegia), G82.0 (flaccid paraplegia), G82.1 (spastic paraplegia), G82.2 (paraparesis and paraplegia, unspecified), G82.3 (flaccid tetraplegia), G82.4 (spastic tetraplegia), and G82.5 (tetraplegia, unspecified).
Data regarding patients' age, sex, etiology of spinal cord injury, level of injury, and the presence of complications were recorded. In cases where complications were present, the time from injury to the development of complications was recorded in months.
Since the most common causes of spinal cord injury differ across age groups, age categories were defined as ≤29 years, 30-44 years, 45-59 years, 60-74 years, and ≥75 years. Etiological classification was based on the most common causes reported in the literature, including traffic accidents, falls from height, sports-related injuries, post-disc herniation or surgery, non-traumatic/inflammatory causes, and other causes.
As the level of injury affects both clinical presentation and the development of complications, injury levels were categorized as cervical (C1-C8), thoracic (T1-T12), and lumbosacral (L1-S5). Evaluation parameters and grouping methods were determined based on similar studies reported in the literature.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patient data regarding age, gender, etiology of spinal cord injury, level of injury, and whether complications develop will be recorded.
Time frame: 1 month
-Average age and gender of patients followed up in our clinic due to spinal cord injury
Time frame: 1 month
Etiology of injury in patients followed up in our clinic due to spinal cord injury
Time frame: 1 month
-Stage of injury in patients followed up in our clinic due to spinal cord injury
Time frame: 1 month
-Whether or not complications developed in patients followed up in our clinic due to spinal cord injury
These complications include: Pressure ulcer, Urinary tract infection, Deep vein thrombosis, Joint contracture, Osteoporosis/fracture, Spasticity, Autonomic dysreflexia, Psychological problems, Sexual problems, Charcot joint, Urethral stricture, Post-traumatic syringomyelia, Heterotopic ossification, Other systemic problems (respiratory problems, cardiac problems, gastrointestinal problems, metabolic and endocrine problems).
Time frame: 1 month
Contact information is provided by the study sponsor or research team.
Naime Meriç KONAR EROL, Associate Professor
CONTACT
Nurten NAS KIRDAR, Assistant Professor
CONTACT
Bandırma Onyedi Eylül University
Other
Epidemiological Evaluation and Complications of Spinal Cord Injury Patients Admitted to Our Clinic: A Retrospective Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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