Ignite Creation Date:
2024-05-06 @ 7:30 PM
Last Modification Date:
2024-10-26 @ 3:08 PM
Study NCT ID:
NCT06035692
Status:
RECRUITING
Last Update Posted:
2024-02-28
First Post:
2023-06-27
Brief Title:
Application of Brachial Plexus Block in Patients Undergoing Cerebral Aneurysm Embolization Via Transradial Approach
Sponsor:
The First Affiliated Hospital with Nanjing Medical University
Organization:
The First Affiliated Hospital with Nanjing Medical University
Study Overview
Official Title:
Effect of Brachial Plexus Block on Outcomes of Upper Extremity Arteries After Intracranial Aneurysm Interventional Surgery Via Transradial Access A Randomized Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-02
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:
ABPBCAETRA
Brief Summary:
The aim of this study was toinvestigate the effect of BPB on outcome of upper extremity arteries in patients undergoing interventional embolization of intracranial aneurysms via TRA A multicenter prospective clinical trial was designed The study subjects were patients undergoing cerebral aneurysm embolization with TRA BPB was given in the BPB group patients and no BPB in the control groupThe incidence of radial artery spasm RAS diagnosed by intraoperative angiography and the occurrence of the unfavorable RA for repeated trans-radial interventions TRI diagnosed by vascular ultrasound 1 month after surgery perioperative changes of blood flow parameters in upper limb vesselspostoperative inflammatory factors and complications were observed in the two groups
Detailed Description:
The aim of this study was to investigate the effect of BPB on outcome of upper extremity arteries in patients undergoing interventional embolization of intracranial aneurysms via TRA A multicenter prospective clinical trial was designed and the study subjects were patients undergoing cerebral aneurysm embolization with TRA Participants were randomly assigned to receive Ultrasound-guided BPB with 015 ropivacaine 20ml BPB group or normal saline 20ml Control group in 11ratioThe primary outcomes measured were the incidence of RAS diagnosed by intraoperative angiography and the occurrence of the unfavorable RA for repeated trans-radial interventions TRI diagnosed by vascular ultrasound 1 month after surgerySecondary outcomes included the severity of RAS Components of unfavorable RA for repeated TRI intraoperative nitroglycerin use Intraoperative hypotension surgeon satisfaction scores
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