Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05161377

Middle Cerebral Artery Aneurysm Trial

Led by University of Alberta · Updated on 2026-03-13

400

Participants Needed

1

Research Sites

815 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Intracranial aneurysms located on the middle cerebral artery (MCA) are considered by many surgeons to represent a distinct subgroup of aneurysms for which clipping may still be the best management option. Most MCA aneurysms are accessible, proximal control can readily be secured in case of rupture, and clip application can typically proceed without requiring the dissection of perforating arteries. In comparison, certain anatomic features of MCA aneurysms such as a wide neck, often including a branch artery origin, frequently render endovascular management more difficult. New endovascular devices were and continue to be introduced to address these anatomic difficulties, including stents, flow diverters, and intra-saccular flow disruptors (ISFDs) such as the WEB. Thus, while most aneurysms are increasingly treated with endovascular methods, many MCA aneurysm patients are still managed surgically, but convincing evidence of which management paradigm is best is lacking.

CONDITIONS

Official Title

Middle Cerebral Artery Aneurysm Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients at least 18 years of age
  • At least one documented, intradural, intracranial aneurysm anywhere on the course of the MCA vessel, ruptured or unruptured
  • Untreated ruptured aneurysm suspected to have occurred more than 30 days prior to inclusion considered unruptured
  • In the case of subarachnoid hemorrhage (SAH), World Federation of Neurosurgical Societies (WFNS) grade 4 or less
  • Patient and aneurysm considered appropriate for either surgical or endovascular treatment by the treating team
Not Eligible

You will not qualify if you...

  • Absolute contraindications to administration of any type of contrast material
  • Patients with arteriovenous malformation (AVM)-associated aneurysms
  • Patients or caregivers unable to provide consent
  • Poor grade (WFNS 5) ruptured aneurysms

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Alberta

Edmonton, Canada

Actively Recruiting

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Research Team

S

Sudeshna Bhattacharyna

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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