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Recruiting NCT06523426

NCT06523426 Ambulatory Geriatric Endoscopic Spine

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Clinical Trial Summary
NCT ID NCT06523426
Status Recruiting
Phase —
Sponsor University Hospital, Bordeaux
Condition Lumbar Decompression
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2024-09-18
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 75 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Patient treated by spinal endoscopy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 50 participants in total. It began in 2024-09-18 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The research focuses on evaluating the clinical outcomes of endoscopic lumbar decompression surgery performed in an outpatient setting for patients over 75 years old. This prospective, multicentric, non-interventional study aims to assess the feasibility and effectiveness of endoscopic techniques, specifically biportal and uniportal approaches, in reducing operative morbidity and hospital stay duration within this demographic. The primary objective is to determine the success rate of outpatient treatment using these endoscopic procedures in elderly patients

Eligibility Criteria

Inclusion Criteria: * Patient aged over 75 years. * Patient consulting for a medical condition involving a spinal pathology at the center, for which endoscopic lumbar decompression on one level is indicated. Exclusion Criteria: * Patients under guardianship or trusteeship. * Individuals deprived of liberty by judicial or administrative decision. * Individuals undergoing psychiatric treatment under constraint requiring consent from a legal representative. * Individuals admitted to a health or social institution for purposes other than research. * Individuals unable to give consent. * Individuals under legal protection. * Patients not affiliated with a social security system. * Patients suffering from infectious, traumatic, or tumoral spinal pathology.

Contact & Investigator

Central Contact

Benjamin BOUYER, PROF

✉ b.bouyer@chu-bordeaux.fr

📞 +335 56 79 87 18

Principal Investigator

Benjamin BOUYER, PROF

PRINCIPAL INVESTIGATOR

University Hospital, Bordeaux

Frequently Asked Questions

Who can join the NCT06523426 clinical trial?

This trial is open to participants of all sexes, aged 75 Years or older, studying Lumbar Decompression. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06523426 currently recruiting?

Yes, NCT06523426 is actively recruiting participants. Contact the research team at b.bouyer@chu-bordeaux.fr for enrollment information.

Where is the NCT06523426 trial being conducted?

This trial is being conducted at Bordeaux, France, Bruges, France, Saint-Jean-de-Védas, France, Saint-Jean-de-Védas, France.

Who is sponsoring the NCT06523426 clinical trial?

NCT06523426 is sponsored by University Hospital, Bordeaux. The principal investigator is Benjamin BOUYER, PROF at University Hospital, Bordeaux. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology