Diabetes and prediabetes in adults preparing for first lumbar spine surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, longitudinal, single-center observational project enrolling adults who are candidates for their first lumbar spine operation. Participants undergo routine preoperative fasting blood glucose and glycated hemoglobin (HbA1c) measurements and complete standard self-administered questionnaires, with all data collected during regularly scheduled consultations. No additional tests are imposed, and the study does not change clinical management or the physician–patient relationship. Collected data will be used to estimate the prevalence of diabetes and prediabetes in this surgical population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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

Exclusion Criteria:

* 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

Where it's running

• Hôpital Privé Jacques Cartier
  Massy, France Recruiting

Study contacts

• Study coordinator: Raphaël PIETTON, MD
• Email: drraphaelpietton@gmail.com
• Phone: 01 60 13 60 60

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.