Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06621836
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-07-12
Brief Title:
Analgesic Efficacy of Intermediate Cervical Plexus Block in Patients Undergoing Neck Surgeries A Comparison Between Two Bupivacaine Concentrations
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Analgesic Efficacy of Intermediate Cervical Plexus Block in Patients Undergoing Neck Surgeries A Comparison Between Two Bupivacaine Concentrations
Status:
COMPLETED
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Cervical plexus blocks CPB have been widely used to provide effective anesthesia and analgesia during various head and neck procedures The ICPB was considered a good alternative to the deep CPB with an easier technique and fewer adverse events such as intravascular epidural subarachnoid injection and phrenic nerve palsy A recent randomized trial investigated the analgesic efficacy of superficial vs intermediate CPB combined with GA during total thyroidectomy Authors used 10 ml bupivacaine 025 bilaterally and they revealed a lower pain score and prolonged duration of analgesia with ICPB compared to superficial CPB however the authors did not assess the influence of this bupivacaine concentration on the diaphragmatic motion 5 This randomized comparative trial is designed to investigate the analgesic efficacy of ICPB combined GA using two bupivacaine concentrations in patients undergoing neck surgeries total thyroidectomy or total laryngectomy We hypothesize that a smaller concentration of bupivacaine 0185 could provide an equivalent analgesic effect to a larger concentration 025 with less impact on the diaphragmatic motion The primary endpoint is the duration of postoperative analgesia The secondary endpoints are the intraoperative hemodynamics the postoperative pain score total postoperative opioid consumption over 24 hours diaphragmatic motions and hemi-diaphragmic paresis
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None