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Intracranial Aneurysm clinical trials

View clinical trials related to Intracranial Aneurysm.

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NCT ID: NCT03140020 Enrolling by invitation - Aneurysm Clinical Trials

Cognition and Functional Connectivity After Elective Treatment of Brain Aneurysms

Start date: January 8, 2018
Phase: N/A
Study type: Observational

The aim of this proposal is to investigate the effects of uneventful microsurgical and endovascular treatment of unruptured saccular non-giant anterior communicating artery [ACoA] aneurysms on resting state functional connectivity levels of higher order cognitive networks and to correlate the connectivity levels of these networks with neuropsychological performance and functional outcome. This study compares two treatment groups and one control group.

NCT ID: NCT03133624 Recruiting - Clinical trials for Intracranial Aneurysm

A Study on a Multidimensional Prediction Model for Rupture Risk of Unruptured Intracranial Aneurysms

CIAP-2
Start date: May 1, 2017
Phase:
Study type: Observational [Patient Registry]

This is a registry study on a multidimensional prediction model for rupture risk of unruptured intracranial aneurysms in China.

NCT ID: NCT03133598 Not yet recruiting - Clinical trials for Un-ruptured Intracranial Aneurysm,Interventional Therapy,Craniotomy

Study of Treatment of Unruptured Intracranial Aneurysms in China

Start date: May 1, 2017
Phase: N/A
Study type: Observational

Un-ruptured intracranial aneurysm is a complex disease that seriously affects human life and health. At present, the treatment of intracranial aneurysm is divided into interventional treatment and craniotomy clipping, the two treatment methods are different in the intervention effect of aneurysm, for example, the complications of interventional therapy are lower than craniotomy clipping, but the long-term patency rate is lower than craniotomy clipping, and there is no standard of treatment in different parts of aneurysm in our country, the choice of intervention measures of un-ruptured aneurysm is different in different clinical centers; on the other hand, there are serious problems in the treatment of aneurysms, because without the relevant guidelines of diagnosis and treatment of intracranial aneurysms, different clinical centers will cause excessive treatment of un-ruptured aneurysms, not only bring unreasonable utilization of medical resources, but also cause the subject's life and property to be threatened. The patients with un-ruptured intracranial aneurysm(n=1500) were included in prospective cohort study, after clipping and intervention operation, setting fixed time for postoperative follow-up, the clinical data and image data were recorded, the safety, efficacy and economic benefits of interventional treatment and craniotomy clipping were compared, providing strategies for the standardized treatment of un-ruptured intracranial aneurysms.

NCT ID: NCT03123302 Completed - Clinical trials for Intracranial Aneurysm

Our Anesthesia Experience During MRI Scan

Start date: February 1, 2017
Phase:
Study type: Observational

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.

NCT ID: NCT03117803 Recruiting - Clinical trials for Aneurysm, Intracranial

The Natural Course of Unruptured Intracranial Aneurysms in a Chinese Cohort

Start date: May 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a registry study of the natural course of unruptured intracranial aneurysms (UIA). In addition, the investigators will analyze the risk factors for the rupture of the UIA and their joint effect. The investigators aim to use research data to create a China national database of UIA.

NCT ID: NCT03087383 Recruiting - Clinical trials for Unruptured Cerebral Aneurysm

Identification of Genetic Polymorphisms Related to Propofol Requirement and Recovery Through Genome-wide Association Study (GWAS) in Total Intravenous Anesthesia for Clipping of Unruptured Cerebral Aneurysm in Korean Population

Start date: March 2, 2017
Phase:
Study type: Observational

In neurosurgical anesthesia, propofol based total intravenous anesthesia (TIVA) is frequently used due to brain relaxation and less effect on electrophysiologic monitoring. Response to propofol can vary between individuals and be associated with clinical factors including age and weight, and genetic polymorphism. Because the importance of rapid recovery in neurosurgery with long operation time is emphasized recently, the choice and dose adjustment of anesthetics should be determined according to clinical and genetic factors. Recently, researches about genetic variations have been performed with single nucleotide polymorphism (SNP). The aim of this study is to find SNPs associated with propofol recovery and response through genome-wide association study (GWAS) in Korean adult population undergoing propofol based TIVA for clipping of unruptured cerebral aneurysm.

NCT ID: NCT03063541 Recruiting - Clinical trials for Unruptured Intracranial Aneurysms

Acetylsalicylic Acid Plus Intensive Blood Pressure Treatment in Patients With Unruptured Intracranial Aneurysms

PROTECT-U
Start date: September 21, 2017
Phase: Phase 3
Study type: Interventional

Purpose of this study is to assess the hypothesis that a strategy with acetylsalicylic acid (ASA) 100 mg/day, intensive blood pressure treatment (targeted systolic blood pressure below 120 mmHg), and a blood pressure measuring device reduces the risk of aneurysm rupture or growth compared with standard care (i.e. no ASA, blood pressure management according to standard blood pressure management, no blood pressure measuring device)

NCT ID: NCT03040284 Recruiting - Clinical trials for Aneurysmal Subarachnoid Hemorrhage, Familial

Non Invasive Measurements of Intracranial Pressure After Aneurysmal Subarachnoid Hemorrhage

HEMAPIC
Start date: March 2015
Phase: N/A
Study type: Interventional

In patients at risk of increased intracranial pressure (ICP), ICP measurements require invasive transducers, usually with insertion of a catheter into the cranium, or through a spinal tap. These invasive modalities involve risks and pain and they can be done only in specialized care units, with a high associated cost. A novel method for detecting changes in ICP has developed recently. The auditory hair cells emit sounds and electric signals in response to sound, which can be easily detected and measured non-invasively with the help of a microphone probe placed in the external ear canal or regular electrodes. Indeed, the cochlear aqueduct connects the cerebrospinal fluid (CSF) spaces to the inner ear in such a way that ICP and inner-ear fluid pressure equalize within seconds. The evaluation of intracranial hypertension by increased ICP (invasive) is not systematically used after aneurysmal subarachnoid hemorrhage. It is then detected by using routine clinical signs of hydrocephalus or another disorder of cerebrospinal liquid flow, in combination with a standard imaging method (TDM). The measurement of noninvasive ICP could allow earlier detection of hydrocephalus or another disorder of cerebrospinal liquid flow, and evaluate whether the increase in ICP precedes patient clinical worsening and / or imaging.

NCT ID: NCT02999659 Recruiting - Cerebral Aneurysm Clinical Trials

Impact of Acute Cerebral Diseases on the Autonomous Nervous System: Progression and Correlation to Therapy and Outcome

Pupillometry
Start date: December 2016
Phase:
Study type: Observational

The pupilometer determines the alteration of the pupil diameter after a defined light stimulus. In this study data is collected from pupilometer measurements of patients with an acute cerebral disease. The measurements take place during daily neurological routine examinations. The values are compared to outcomes resulting from pupilometer measurements done on patients having not an acute cerebral disease (e.g. cerebral aneurysm without symptoms). The study aims to establish the not invasive method of pupillometry for detecting neurological degradations early.

NCT ID: NCT02998229 Recruiting - Clinical trials for Intracranial Aneurysm

Artisseā„¢ Intrasaccular Device IDE

ARTISSE
Start date: April 16, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of the Artisseā„¢ Intrasaccular Device in the treatment of unruptured and ruptured wide-neck bifurcating intracranial aneurysms.