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Testing the Feasibility of Using Ropivacaine in Spinal Anesthesia for Patients With Lower Back Surgery — SASS  

Anesthesia, Spinal Clinical Trial

Official title:
Testing the Feasibility of Using Ropivacaine in Spinal Anesthesia for Patients With Lower Back Surgery

Clinical Trial Summary

The goal of this pilot clinical trial is to test the feasibility of conducting a randomized controlled trial that will examine the use of ropivacaine in the spinal anesthesia for patients undergoing elective 1- or 2-level lower spine surgery. This study aims to: - Determine the rates of eligibility, recruitment, consent, and attrition - Determine the acceptability among patients, surgeons, anesthesiologists, and nurses of doing spine surgery under spinal anesthesia - Gather preliminary data on outcomes relevant to a future dose-finding study Participants will be randomized to one of three treatment groups: - General anesthesia with endotracheal tube - Spinal anesthesia with bupivacaine - Spinal anesthesia with ropivacaine

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05824338
Study type Interventional
Source Fraser Health
Contact Michelle Mozel, MSc.
Phone 604-520-4253
Email michelle.mozel@fraserhealth.ca
Status Not yet recruiting
Phase Early Phase 1
Start date January 1, 2024
Completion date April 30, 2024
View Details
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