Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06752096

Robot-Assisted Neurovascular Intervention

Led by Navigantis Inc. · Updated on 2026-01-16

10

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

Sponsors

N

Navigantis Inc.

Lead Sponsor

S

Severance Hospital, Yonsie University College of Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

Patients scheduled for neurovascular interventions may be eligible to have their procedure done robotically.

CONDITIONS

Official Title

Robot-Assisted Neurovascular Intervention

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for neurovascular interventions such as diagnostic cerebral angiography for cerebrovascular diseases, arterial embolization for meningioma treatment, or thrombectomy for thrombotic arterial occlusion-induced cerebral ischemia
  • Selection according to the same criteria as standard cerebral angiography and interventional procedures
Not Eligible

You will not qualify if you...

  • Surgery within 4 weeks prior to participation or incomplete recovery from surgery
  • Pregnancy or breastfeeding
  • Existing or expected vasospasm, bleeding, or severe atheromatous disease
  • Allergy to contrast agents used in angiography
  • Renal failure
  • History of myocardial infarction or superior vena cava syndrome within 3 months or existing heart disease
  • Inability to cooperate or express intent to proceed with procedure
  • Severe or life-threatening comorbidities affecting symptom improvement or procedure benefit
  • Non-life-threatening comorbidities preventing proper follow-up
  • For cerebral ischemic stroke patients: ASPECTS score of 0-2 on pre-treatment CT
  • Inability to perform femoral puncture within 60 minutes after CT angiography
  • Absence of femoral pulse
  • Highly challenging vascular access with expected time over 90 minutes from CT angiography to reperfusion
  • Suspected cerebral artery dissection or atherosclerosis as stroke cause
  • Chronic intracranial occlusion based on history or imaging

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

Severence Hospital, Yonsei University College of Medicine

Seoul, Korea, South Korea

Actively Recruiting

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Research Team

K

Ken Lock

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DEVICE_FEASIBILITY

Number of Arms

1

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