Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT04668261

Longitudinal Investigation of Brain Blood Flow Changes in Neurosurgical Patients

Led by University of Zurich · Updated on 2020-12-29

400

Participants Needed

1

Research Sites

356 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Primary study objective: • Longitudinal observation of brain blood flow changes in neurosurgical patients with or without a neurosurgical intervention as compared to a healthy cohort. Secondary study objectives: * Longitudinal observation of hemodynamic patterns versus structural brain tissue changes in neurosurgical patients. * Changes in blood flow patterns and structural brain tissue after neurosurgical interventions as compared to a healthy cohort. * Determining hemodynamic imaging patterns that can be tested as novel imaging markers.

CONDITIONS

Official Title

Longitudinal Investigation of Brain Blood Flow Changes in Neurosurgical Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female subjects over 18 years of age
  • Written informed consent after receiving study information
  • For non-German speakers, presence of a translator with sufficient German language skills
  • Patients with neurosurgical diseases that may affect brain blood flow, including cerebrovascular disease, brain tumors, or normal pressure hydrocephalus
  • Healthy subjects over 18 years of age with informed consent and translator if needed
Not Eligible

You will not qualify if you...

  • Unwilling or unable to cooperate with breathing maneuvers
  • Respiratory or cardiac issues preventing breathing through a mask
  • Medical contraindications to controlled high or low carbon dioxide levels (such as increased intracerebral pressure, metabolic acidosis or alkalosis)
  • Standard MRI scanning contraindications
  • Pregnancy
  • Multiple intracranial diseases
  • Intracranial hemorrhage within the last 3 months
  • Symptomatic increased intracranial pressure
  • For healthy subjects, history or current neurological diseases or deficits

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 Hospital Zurich

Zurich, Switzerland, 8032

Actively Recruiting

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Research Team

J

Jorn Fierstra, MD, PhD

CONTACT

L

Luca Regli, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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