Intracranial Aneurysm Clinical Trial
Official title:
Our Anesthesia Experience During MRI Scan
In this study we aim to investigate the relationship between our anesthesia practice and post procedure complications after MRI scanning with sedation. This is a retrospective, single center observational study. All patients undergoing MRI scan during the study period will be included.
In this study we aim to investigate the influence of patient characteristics and anesthesia
choice on possible complications in patients undergoing MRI under sedation retrospectively.
After one of the routine sedation protocol used in our department was chosen and applied
according to the physical status of the patient and the physicians decision, the datas of the
patients will be recruited to the study from the medical records . Patient characteristics
(age, gender, weight, height), ASA (American Society of Anethesiology) classification,
associated diseases will be recorded . After the procedure was completed all the
complications during the 2 hours waiting period in the recovery room will be recorded from
the medical records. All the complşcation and recovery times will be recorded from the
medical records. Whether the patient received radiocontrast material or not will also be
recorded. The patients will be called by phone, and will be questioned for the complications,
any epileptic seizure attack, or increase in the number of seizures, any admission to
emergency room or any in patient admission to the hospital will be recorded which developed
in the first week after the procedure.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT04870047 -
Coating to Optimize Aneurysm Treatment In The New Flow Diverter Generation
|
N/A | |
| Recruiting |
NCT05968053 -
Detection of Microplastics and Nanoplastics in Neurosurgery Patients (DT-MiNi)
|
||
| Not yet recruiting |
NCT05665309 -
Interest of Pre-operative Use of 3D Printing for Endovascular Treatment of Unruptured Intracranial Aneurysms With Intrasaccular Flow Disruptor
|
N/A | |
| Completed |
NCT02783339 -
Neuroform Atlas Stent for Intracranial Aneurysm Treatment
|
||
| Withdrawn |
NCT01194388 -
Axium Coil in Completing Endovascular Aneurysm Surgery Study
|
||
| Completed |
NCT00071565 -
Familial Intracranial Aneurysm Study II
|
N/A | |
| Recruiting |
NCT05409989 -
MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED™ X™) Post-Approval Study
|
N/A | |
| Completed |
NCT03680742 -
Contour Neurovascular System - European Pre-Market Unruptured Aneurysm
|
N/A | |
| Completed |
NCT04872842 -
Establishment of Online Registration Platform for Unruptured Intracranial Aneurysms Based on 100 Regional Medical Centers in China and Population Follow-up Study
|
||
| Terminated |
NCT02532517 -
Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device
|
N/A | |
| Completed |
NCT03663257 -
Study to Evaluate Cerebral AneurysmFlow Results in Occlusion
|
||
| Recruiting |
NCT06189950 -
Registration Trial of the Intracranial Visualized Stent for the Wide-necked Intracranial Aneurysms:REBRIDGE
|
N/A | |
| Recruiting |
NCT05608122 -
Establishment of Online Registration Platform for Unruptured Intracranial Aneurysms Based on Regional Medical Centers in China and Population Follow-up Study (Phase Ⅱ)
|
||
| Recruiting |
NCT03661463 -
Unruptured Intracranial Aneurysm Aspirin Trial (UIAAT).
|
Phase 2 | |
| Completed |
NCT02609867 -
A Feasibility Study to Evaluate the Safety and Effectiveness of Implantation of Flowise Cerebral Flow Diverter (Flowise)
|
N/A | |
| Active, not recruiting |
NCT02292017 -
Prospective Packing Density With Target Coils I
|
N/A | |
| Active, not recruiting |
NCT01872741 -
Minipterional Versus Pterional Craniotomy
|
N/A | |
| Completed |
NCT00993057 -
Efficiency of Two Glucose Sampling Protocols for Maintenance of Euglycemia
|
Early Phase 1 | |
| Completed |
NCT00777907 -
Complete Occlusion of Coilable Aneurysms
|
Phase 3 | |
| Completed |
NCT00777088 -
Pipeline for Uncoilable or Failed Aneurysms
|
N/A |