Status:
COMPLETED
Interest of the Patient Management by Improved Recovery After Surgery in Percutaneous Vertebroplasty
Lead Sponsor:
GCS Ramsay Santé pour l'Enseignement et la Recherche
Conditions:
Vertebral Compression
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This research aims to demonstrate the benefits of the RAAC program for patients undergoing cementoplasty, in particular on their level of anxiety and pain control throughout the perioperative phase.
Detailed Description
The aim of the study is to compare the preoperative anxiety of patients hospitalized for a percutaneous vertebroplasty, depending on whether or not they are managed in an RAAC program.
Eligibility Criteria
Inclusion
- Age ≥ 80 years or ≥ 18 years with oncological history;
- Patient with vertebral compression fracture with indication for percutaneous vertebroplasty;
- Patient seen in preoperative anesthesia / radiology consultation more than 4 days before the date of the vertebroplasty;
- Having expressed their consent to participate in the study.
Exclusion
- Patient with a contraindication to percutaneous vertebroplasty, such as coagulation disorders, or an allergy or hypersensitivity to any of the products administered during the procedure;
- Patient not affiliated to a social security scheme;
- Patient participating in another clinical trial during the follow-up period;
- Inability to understand information related to the study (linguistic, psychiatric, cognitive reason, etc.).
Key Trial Info
Start Date :
November 17 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 19 2022
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04453163
Start Date
November 17 2020
End Date
December 19 2022
Last Update
January 27 2023
Active Locations (1)
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1
Clinique Belharra
Bayonne, France