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NCT03996148

Time to Post-Anesthesia Neurological Evaluation With Three Different Anesthetic Techniques

Time to Post-Anesthesia Neurological Evaluation and Hemodynamic Stability in Carotid Endarterectomy Comparing Three General Anesthetic Techniques Targeted to a Preset Bispectral Index Value: a Pilot Study
The Cooper Health System·Phase 4·ClinicalTrials.gov·drugCompleted
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Study focus
Disease/Condition
Carotid Artery Stenosis
Drug/Device/Intervention
Remifentanil, Propofol, and Desflurane
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
The Cooper Health System
Location
Camden, United States of America
Timeline & enrollment
Phase
Phase 4
Start date
Sep 29, 2017
End date
Sep 19, 2018
Enrollment
21 participants
Primary outcome

Time to first neurological exam

Summary

The objective of this pilot study is to analyze the differences in time to first
 postoperative neurological examination (cranial nerve XII - tongue movement, movement of
 extremities) and intraoperative hemodynamic stability with three different general anesthetic
 techniques that are used for carotid endarterectomy. Carotid endarterectomy surgery removes
 the plaque and stenosis but has a 1-3% risk of periprocedural stroke or death. The ability to
 detect neurological abnormalities early after surgery is vital in this patient population to
 facilitate timely additional diagnostics or interventions if a potential stroke is detected.
 Anesthetic techniques that facilitate an earlier reliable neurological exam will thus greatly
 benefit this surgical patient population. The primary objective of this pilot study is to
 determine the time difference from end of surgery to first neurologic exam between three
 commonly used anesthetic methods for carotid endareterectomy.

ICD-10 classifications
Occlusion and stenosis of carotid arteryCarotid artery syndrome (hemispheric)Injury of carotid arteryAneurysm and dissection of carotid arteryOcclusion and stenosis of vertebral artery
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03996148
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT03996148 through Pure Global AI's free database. This Phase 4 trial is sponsored by The Cooper Health System and is currently Completed. The study focuses on Carotid Artery Stenosis. Target enrollment is 21 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.