Prevalence of Diabetes in Patients Who Are Candidates for Spine Surgery

ConditionSpine Disease
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

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%.

Time frame
Day 1

Secondary outcomes

1

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).

Time frame
Day 0
2

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).

Time frame
Month 3
3

Radicular pain

Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).

Time frame
Day 0
4

Radicular pain

Pain will be assessed by the patient on a visual analog scale from 0 to 10 (0 = no pain, 10 = maximum pain).

Time frame
Month 3

Other outcomes

Sponsors and contacts

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