Cerebral Aneurysm

8

Review clinical trials related to Cerebral Aneurysm. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Sirolimus on Molecular Alterations in Cerebral Aneurysms

The objective of this study is to explore the effects of Sirolimus on the underlying molecular alterations of cerebral aneurysms.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

Clipping of an unruptured cerebral artery aneurysm [+3]

Dissecting, traumatic, or mycotic brain aneurysm. [+10]

Status: Not yet recruiting

NIRS and BIS Monitoring During Cerebral Aneurysm Coiling

This prospective observational study aims to evaluate the effectiveness of Near-Infrared Spectroscopy (NIRS) and Bispectral Index (BIS) monitoring during endovascular coil embolization of cerebral aneurysms under general anesthesia. Changes in regional cerebral oxygen saturation (rSO₂) measured by NIRS will be assessed in relation to BIS values and hemodynamic parameters throughout the procedure. The frequency, duration, and severity of cerebral desaturation episodes detected by NIRS, as well as their association with anesthetic depth and hemodynamic fluctuations, will be analyzed. The study does not involve any additional intervention beyond routine clinical monitoring.

Participants needed: 75
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Dokuz Eylul UniversityUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Age ≥18 years [+4]

Refusal or inability to provide informed consent [+6]

Status: Not yet recruiting

Parent Artery Reconstruction for Small Unruptured Cerebral Aneurusms Using Flow DiverTers: a Multicenter Randomized Trial(PARAT-MT)

A prospective, multicenter, randomized controlled clinical trial with open-label treatment and blinded endpoint assessment.

Participants needed: 1,008
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Changhai HospitalUpdated: Jan 3, 2025
Eligibility criteria

Age 18-75 years. [+3]

Subjects with two or more multiple aneurysms requiring treatment within one year... [+15]

Status: Not yet recruiting

Clinical Trial for the Validation of AR Based Neuronavigation System

The goal of this clinical trial is to test augmented reality (AR) based neuronavigation system in surgeries for patients of brain neoplasm or cerebral vascular disease. The main questions it aims to answer are: • AR based neuronavigation system can achieve accuracy that is not inferior to conventional intraoperative navigation system. Participants will participate the study after informed consent. When participants undergo surgery for their brain tumor, we will set up 2 types of neuronavigation, conventional navigation system and developed AR based neuronavigation system. Surgeon will plan and conduct surgery based on only conventional navigation system, but 3D errors at several selected points between two types of navigation will be measured and analyzed.

Participants needed: 80
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Seoul National University HospitalUpdated: Dec 3, 2024Locations: 1
Eligibility criteria

Adult patients aged 18 years or older who underwent MRI or CT scan due to brain... [+1]

Cases where application of navigation is not necessary according to the judgment... [+2]

Status: Recruiting

Prospective, Single-Arm, Multicenter Study to Evaluate the Effectiveness and Safety of Endovascular Treatment in Patients With Cerebral Aneurysms Using P64 and P48 Flow-Diverter Stents

The use of flow-diverting stents for the endovascular treatment of cerebral aneurysms has proven to be effective and efficient in several clinical studies, leading to its widespread adoption. Devices with a higher number of filaments have a greater flow-diverting effect and less variation when there are changes in the caliber of the underlying vessel or in curved vessels. However, ischemic complications secondary to their implantation have been reported, prompting the development of various strategies to reduce their thrombogenicity. Phenox is the only company to date that has developed an anti-thrombogenic coating, known as HPC (Hydrophilic Polymer Coating), which, when applied to the p64 MW HPC and p48 MW HPC devices, has shown to reduce the likelihood of thromboembolic complications associated with their implantation.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hospital Universitario Central de AsturiasUpdated: Nov 22, 2024Locations: 11
Eligibility criteria

Patients over 18 years old with incidental, symptomatic, and/or ruptured cerebra... [+1]

Patients under 18 years of age. [+3]

Status: Recruiting

The RISE Trial: A Randomized Trial on Intra-Saccular Endobridge Devices

Intracranial bifurcation aneurysms are commonly repaired with surgical and with endovascular techniques. Wide-necked bifurcation aneurysms (WNBA) are a difficult subset of aneurysms to successfully repair endovascularly, and a number of treatment adjuncts have been designed. One particularly promising innovation is the WEB (Woven EndoBridge), which permits placement of an intra-saccular flow diverting mesh across the aneurysm neck, but which does not require anti-platelet agent therapy. Currently, which treatment option leads to the best outcome for patients with WNBA remains unknown. There is a need to offer treatment with the WEB within the context of a randomized care trial, to patients currently presenting with aneurysms thought to be suitable for the WEB.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre hospitalier de l'Université de Montréal (CHUM)Updated: Aug 15, 2024Locations: 4
Eligibility criteria

patient with an intracranial aneurysm in whom WEB is considered an appropriate t... [+4]

Absolute contraindication to surgery, endovascular treatment or anesthesia [+3]

Status: Recruiting

Epidemiological Insights Into the Formation, Progression, and Rupture of Intracranial Aneurysms: A Retrospective, Multi-Center Hospital-Based Study in China

This is a retrospective, hospital-based and multi-center study aiming at investigating the potential exposures associated with the formation, progression, and rupture of intracranial aneurysms in Chinese population.

Participants needed: 30,000
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Zhujiang HospitalUpdated: Jun 13, 2024Locations: 1
Eligibility criteria

IA diagnosis (ruptured or unruptured) or exclusion by digital subtractive angiog... [+3]

Missing data of age, sex or hypertensive status; [+4]

Status: Recruiting

Registry of Multicenter Brain-Heart Comorbidity in China

This study is a multi-center, prospective, registry study. This research was supported by the National Key Research and Development Program. To establish a domestic multi-center, large-scale "brain-heart comorbidity" dynamic database platform including clinical, sample database, image and other multi-dimensional information requirements, through the construction of a multi-center intelligent scientific research integration platform based on artificial intelligence. Any of newly diagnosed cardiovascular related diseases were identified via ICD-10-CM codes: I21, I22, I24 (Ischaemic heart diseases) \[i.e., ACS\], I46 (cardiac arrest), I48 (Atrial fibrillation/flutter), I50 (Heart failure), I71 (Aortic disease), I60 (subarachnoid hemorrhage), I61 (intracerebral hemorrhage), I63 (Cerebral infarction), I65 (Occlusion and stenosis of precerebral arteries), I66 (Occlusion and stenosis of cerebral arteries), I67.1 (cerebral aneurysm), I67.5 (moyamoya diseases), Q28.2 (Arteriovenous malformation of cerebral vessels). The data is stored on the brain-heart comorbidity warehouse via a physical server at the institution's data centre or a virtual hosted appliance. The brain-heart comorbidity platform comprises of a series of these appliances connected into a multicenter network. This network can broadcast queries to each appliance. Results are subsequently collected and aggregated. Once the data is sent to the network, it is mapped to a standard and controlled set of clinical terminologies and undergoes a data quality assessment including 'data cleaning' that rejects records which do not meet the brain-heart comorbidity quality standards. The brain-heart comorbidity warehouse performs internal and extensive data quality assessment with every refresh based on conformance, completeness, and plausibility (http://10.100.101.65:30080/login).

Participants needed: 100,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Beijing Tiantan HospitalUpdated: Sep 21, 2023Locations: 14
Eligibility criteria

age > 18 years old [+1]