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Opioid Sparing Anesthesia in Cervical Spine Surgery

NCT05717361 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-02-08

No results posted yet for this study

Summary

The aim of this double blind randomized study will be to investigate the effect of an opioid-free anesthesia regimen with a mixture of lidocaine and ketamine in the same syringe versus remifentanyl analgesia in cervical spine surgery.

Conditions

  • Pain, Postoperative
  • Pain, Acute
  • Pain, Chronic
  • Pain, Nociceptive
  • Ketamine
  • Lidocaine
  • Analgesia
  • Analgesics
  • Cervical Spine Surgery

Interventions

DRUG

ketamine-lidocaine

In the KL group, patients will be administered in a total volume of 20 mL,1mL/10 kg of the solution containing ketamine, lidocaine at predefined concentrations. As maintenance, they will be receiving 1mL/10kg/h of the aforementioned solution

DRUG

Remifentanil

In the Remifentanil group, patients will be administered in a total volume of 20 mL, 2 mcg/kg of fentanyl. As maintenance, they will be receiving 1 mL/10kg/h of a remifentanil solution

Sponsors & Collaborators

  • Aretaieion University Hospital

    collaborator OTHER

  • Evangelismos Hospital

    lead OTHER

Principal Investigators

  • Kassiani Theodoraki · Aretaieion University Hospital, Athens, Greece

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-01
Primary Completion
2024-11-01
Completion
2024-11-01

Countries

  • Greece

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05717361 on ClinicalTrials.gov