About this trial
The purpose of the study is to assess, through systematic screening, the prevalence of diabetes or prediabetes in patients who are candidates for lumbar spine surgery.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients,
Patients who have been informed of the research and have not indicated their opposition to the use of their medical data,
Patients who are candidates for their first lumbar spine surgery, whether instrumented or not
Disqualifiers
Non-instrumented percutaneous surgery (cementoplasty)
Presence of spinal osteosynthesis equipment
Surgery performed for an infectious or tumoral spinal condition
Surgery via an anterior or lateral approach
Trial population
Population of patients who are candidates for lumbar spine surgery
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Diabetes or prediabetes présence
Diabetes is defined as a blood glucose level of at least 1.26 g/L and a glycated hemoglobin level greater than or equal to 6.5%. Prediabetes is defined as a blood glucose level greater than 1.10 g/L and less than 1.26 g/L and a glycated hemoglobin level between 5.7% and 6.4%.
Secondary outcomes
Low back pain
Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).
Low back pain
Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).
Radicular pain
Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).
Radicular pain
Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).
Sponsors and contacts
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