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Clinical Trial Summary

The aim of this study is to assess the efficacy of the ARISTA AH for restoring hemostasis following a long segment posterior spinal fusion.


Clinical Trial Description

After being informed about the study and potential risks, all patients giving written inform consent will be included in the study during their preoperative visit. After eligibility criteria checking and based on their respective surgical indication, participants will be randomized in a single-blinded and stratified manner (participant only) in a 1:1 ratio to ARISTA-AH or no ARISTA-AH. The stratification process will consider the number of instrumented vertebra during each surgery (level 1: 5 to 8 vertebra; level 2: 9 or more instrumented vertebra). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05323448
Study type Interventional
Source Polyclinique Bordeaux Nord Aquitaine
Contact Stéphane BOURRET
Phone +33556437017
Email s.bourret@bordeauxnord.com
Status Recruiting
Phase N/A
Start date October 25, 2022
Completion date December 1, 2024

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