Ignite Creation Date:
2024-05-06 @ 3:51 PM
Last Modification Date:
2024-10-26 @ 1:58 PM
Study NCT ID:
NCT04784078
Status:
UNKNOWN
Last Update Posted:
2021-04-13
First Post:
2021-03-03
Brief Title:
Randomized Comparison of Distal Radial Versus Conventional Radial Access for Coronary Angiography and Intervention
Sponsor:
Beijing Anzhen Hospital
Organization:
Beijing Anzhen Hospital
Study Overview
Official Title:
Randomized Comparison of Distal Radial Versus Conventional Radial Access for Coronary Angiography and Intervention
Status:
UNKNOWN
Status Verified Date:
2021-04
Last Known Status:
NOT_YET_RECRUITING
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:
Distal radial access dTRA represents a novel site for radial artery access in interventional cardiology there is little data compare dTRA with conventional radial access cTRA in a randomized manner
It aims to randomly compare between the new distal radial access via the snuffbox and the conventional radial access for percutaneous coronary intervention PCI and angioplasty procedures The objectives of comparing both procedures are to analyze the frequency of complications in terms of occlusion arterial spasm hematoma and to weigh accesses effectiveness in terms of time and attempts to puncture crossover rate procedure duration hemostasis time
Candidates for coronary angiography are being randomized into the interventional group to undergo the angiography through the distal radial artery as the access site or the control group accessing through the radial artery Procedural and post procedural outcomes and complications are being reported while patients are in hospital All patients undergo doppler ultrasonography within 24 hours before and after the procedure 4 weeks after procedure
It aims to randomly compare between the new distal radial access via the snuffbox and the conventional radial access for percutaneous coronary intervention PCI and angioplasty procedures The objectives of comparing both procedures are to analyze the frequency of complications in terms of occlusion arterial spasm hematoma and to weigh accesses effectiveness in terms of time and attempts to puncture crossover rate procedure duration hemostasis time
Candidates for coronary angiography are being randomized into the interventional group to undergo the angiography through the distal radial artery as the access site or the control group accessing through the radial artery Procedural and post procedural outcomes and complications are being reported while patients are in hospital All patients undergo doppler ultrasonography within 24 hours before and after the procedure 4 weeks after procedure
Detailed Description:
None
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