Ignite Creation Date:
2024-05-06 @ 6:59 PM
Last Modification Date:
2024-10-26 @ 2:58 PM
Study NCT ID:
NCT05851274
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-05-09
First Post:
2023-04-12
Brief Title:
Transradial Access for Ruptured Intracranial Aneurysms Embolization
Sponsor:
The First Affiliated Hospital with Nanjing Medical University
Organization:
The First Affiliated Hospital with Nanjing Medical University
Study Overview
Official Title:
Transradial Access for Ruptured Intracranial Aneurysms Embolization--A Multicentre Randomised Open-labelNon-inferiority Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-04
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:
TRA-RIA
Brief Summary:
The goal of this clinical trail is to compare the difference between transradial access TRA and transfemoral accessTFA for ruptured intracranial aneurysms embolization The main question it aims to answer is whether is TRA not inferior to TFA In the experimental group the transradial access TRA was used which was to puncture the radial artery and insert a radial sheath to establish a surgical pathway for embolization of the aneurysm In the control group transfemoral access TFA was used to embolize the aneurysms which was to puncture the femoral artery and insert the femoral sheath to establish a surgical pathway for embolizing the aneurysmsThe two groups of patients received an oral loading dose of aspirin 300mg plus clopidogrel 300mg on the day of surgery while patients who were unable to take orally were given nasal feeding During the operation systemic heparinization was performed with a starting dose of 75Ukg intravenous injection and the injection was halved every 1h until 1000U After the operation protamine neutralizing heparin 1mg protamine neutralizing 100U heparin was used
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