Actively Recruiting
Prevalence of Diabetes in Patients Who Are Candidates for Spine Surgery
Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2025-06-12
500
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating how common diabetes and prediabetes are among patients who are planning to have lumbar spine surgery. This observational study is conducted at a single center and follows patients over time without changing their usual medical care or physician relationships. The study focuses on patients undergoing their first lumbar spine surgery and aims to better understand the prevalence of these conditions in this specific group. During the study, patients will have their fasting blood glucose and glycated hemoglobin levels measured as part of their standard preoperative assessments. Questionnaires completed by patients about their health and symptoms are also collected routinely. No additional treatments or interventions are given as part of the study, and the research is based on observations during regular medical visits. Participants will be involved during their scheduled consultations where their blood tests and questionnaires are reviewed. The main outcome measured is the presence of diabetes or prediabetes on the day of surgery. Secondary outcomes include assessments of low back pain, radicular pain, and the functional impact of the spinal condition at the time of surgery and three months later. The study spans from before surgery through follow-up to monitor these health aspects.
CONDITIONS
Brief Title
Prevalence of Diabetes in Patients Who Are Candidates for Spine Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Assessments take place during routinely scheduled consultations.
Duration - Up to 3 months
Participants who undergo routine lumbar spine surgery are observed during their standard preoperative and postoperative care. Measurements such as fasting blood glucose, glycated hemoglobin, and patient questionnaires are collected as part of routine care.
Visits occur during routine clinical consultations before surgery and at 3 months after surgery.
Trial Site Locations
Total: 1 location
1
Hôpital Privé Jacques Cartier
Massy, France, 91300
Actively Recruiting
Research Team
R
Raphaël PIETTON, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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