Ignite Creation Date:
2024-05-06 @ 6:52 PM
Last Modification Date:
2024-10-26 @ 2:56 PM
Study NCT ID:
NCT05816109
Status:
RECRUITING
Last Update Posted:
2023-04-18
First Post:
2023-01-19
Brief Title:
The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery
Sponsor:
Aydin Adnan Menderes University
Organization:
Aydin Adnan Menderes University
Study Overview
Official Title:
The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery
Status:
RECRUITING
Status Verified Date:
2023-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery
Detailed Description:
The study was designed as a double-blind prospective randomized controlled trial
Blindness The healthcare professionals who will monitor the patients 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 30min161224 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
Blindness The healthcare professionals who will monitor the patients 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 30min161224 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None