Clinical Trials Directory

Trials / Completed

CompletedNCT05577559

Ultrasound-Guided Intermediate Cervical Plexus or Cervical Erector Spinae Block for Anterior Cervical Spine Surgery

Regional Analgesia Using Ultrasound-Guided Intermediate Cervical Plexus Block or Cervical Erector Spinae Block for Anterior Cervical Spine Surgery: A Randomized Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
58 (actual)
Sponsor
Zagazig University · Other Government
Sex
All
Age
21 Years – 60 Years
Healthy volunteers
Accepted

Summary

• Neck pain and stiffness or sore throat, are common after anterior cervical spine surgery. Complications are rare but can be serious and even potentially life-threatening if they do occur. Rapid recovery and emergence from general anesthesia are important in cases of anterior cervical spine surgery.

Detailed description

* Null hypothesis (H0): No difference between the regional analgesia effects of bilateral ultrasound-guided superficial cervical plexus block and bilateral cervical erector spinae block in patients undergoing anterior cervical spine surgery under general anesthesia. * Alternative hypothesis (H1): There are differences between the regional analgesia effects of bilateral ultrasound-guided superficial cervical plexus block and bilateral cervical erector spinae block in

Conditions

Interventions

TypeNameDescription
PROCEDUREintermediate cervical plexus blockpatients will receive bilateral ultrasound guided intermediate cervical plexus block using 15 ml of bupivacaine 0.25% for each side.
PROCEDURECervical Erector spinae blockpatients will receive bilateral ultrasound guided cervical erector spinae plane block using 15 ml of bupivacaine 0.25% for each side at the level of C6.

Timeline

Start date
2022-11-01
Primary completion
2023-12-01
Completion
2023-12-01
First posted
2022-10-13
Last updated
2023-12-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05577559. Inclusion in this directory is not an endorsement.