The Effect of Superficial Cervical Plexus Block on Postoperative Recovery

Status Recruiting

Clinical Trial Summary

The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery

Clinical Trial Description

The study was designed as a double-blind, prospective randomized controlled trial. Blindness; The healthcare professionals who will monitor the patient's pain in the post-operative period will not know whether the superficial cervical plexus block is applied to the patients. Randomization of the patients was planned using computer aided. It is envisaged that 20 participants will be included in the patient group that will have a superficial cervical plexus block and will not have a superficial cervical plexus block. The current pain status in the postoperative period in the patient groups that will or will not have a superficial cervical plexus block is determined by NRS (Numerical rating scale) at rest and in motion at certain hour intervals ( 30.min,1.,6.,12.,24. hours) will be done, when the patients' NRS scores are 4 and above, an additional intravenous analgesic will be administered, and the number of bolus doses with PCA in the first 24 hours will be recorded. The quality of recovery (QoR-40) scoring system will be evaluated at the postoperative 24th hour of both patients with and without superficial cervical plexus block. In addition, the hemodynamic values of the patients will be recorded in these intervals. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05816109
Study type	Interventional
Source	Aydin Adnan Menderes University
Contact	Büsra CEYHAN CAN, Resident
Phone	+902564441256
Email	busraceyhancan@gmail.com
Status	Recruiting
Phase	N/A
Start date	May 1, 2023
Completion date	February 1, 2024

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