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Clinical Trials/KCT0008461
KCT0008461
Recruiting
未知

Comparing the effects of applying a multimodal analgesic strategy including cervical plexus block to improve postoperative pain management in patients undergoing carotid endarterectomy: a randomized, observer-blinded trial

Samsung Medical Center0 sites40 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Samsung Medical Center
Enrollment
40
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Adult patients undergoing elective carotid endarterectomy under general anesthesia (aged between 20 and 80 years of age)
  • •2\. American Society of Anesthesiologists (ASA) physical status classification (ASA class) I\- III
  • •3\. A person who consented to the clinical trial and signed the subject consent form

Exclusion Criteria

  • •1\. Children under the age of 19, adults over the age of 80
  • •2\. Patients who refused cervical plexus block
  • •3\. Patients with neurological abnormalities
  • •4\. Patients with bleeding abnormalities or disabilities
  • •5\. Those who cannot undergo nerve block surgery due to recent systemic or partial infection
  • •6\. Patients who have taken opioids for a long time, patients with a history of severe side effects to opioids
  • •7\. Patients allergic to local anesthetics
  • •8\. A person who is judged to be inappropriate to participate in a clinical trial according to the judgment of the researcher
  • •9\. Patients with a history of previous CEA surgery
  • •10\. Patients who have failed cervical plexus block

Outcomes

Primary Outcomes

Not specified

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