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Longitudinal Investigation of Brain Blood Flow Changes in Neurosurgical Patients

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Enrolling

Conditions

Brain Blood Flow Impairment

Treatments

Other: Advanced imaging investigation

Study type

Observational

Funder types

Other

Identifiers

NCT04668261
2020-02314

Details and patient eligibility

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.

Full description

Primary study objective:

• to study the longitudinal observation of brain blood flow changes in neurosurgical patients to evaluate the effect of surgical or conservative treatment on the brain structural and hemodynamic integrity.

Secondary study objectives:

  • To observe the relationship between longitudinal changes in hemodynamic patterns and structural brain tissue changes in neurosurgical patients.
  • To determine different hemodynamic patterns that may be used as novel imaging biomarkers in future studies.

4.2 Outcomes

Outcomes of the project:

Primary endpoint:

To find correlation between course of disease, neurosurgical intervention and changes in brain blood flow and brain structure.

Secondary endpoints:

  • Correlation between progression of disease and hemodynamic patterns over time (ie. novel imaging markers)
  • Correlation of clinical management (neurosurgical treatment vs. best medical care) and changes in brain blood flow.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

Patients:

  • Male and Female subjects >18 years of age

  • Written informed consent after participants' information. Foreign speaking patients should be accompanied by a person with sufficient German language proficiency to act as a translator

  • Neurosurgical diseases with the potential to alter blood flow to the brain:

    • Cerebrovascular disease
    • Brain tumors
    • Normal Pressure Hydrocephalus

Healthy subjects:

  • Male and Female subjects >18 years of age
  • Written Informed Consent by the participant after information about the project. Foreign speaking healthy subjects should be accompanied by a person with sufficient German language proficiency to act as a translator

Exclusion criteria:

Patients:

  • Unwilling or unable to co-operate with breathing maneuvers
  • Respiratory or cardiac limitations to breathing through a mask
  • Medical contra-indications to limited hypercapnia (high CO2 - 50 mmHg) or hypocapnia (low CO2 - 30 mmHg) (i.e., known increased intracerebral pressure, metabolic acidosis or alkalosis)
  • Standard contraindications for MRI scanning
  • Verbal confirmed pregnancy
  • Known multiple intracranial diseases
  • Presence of intracranial hemorrhage within the last 3 months
  • Symptomatic increased intracranial pressure

Healthy subjects:

  • Unwilling or unable to co-operate with breathing maneuvers
  • Respiratory or cardiac limitations to breathing through a mask
  • Medical contra-indications to limited hypercapnia (high CO2 - 50 mmHg) or hypocapnia (low CO2 - 30 mmHg) (i.e., known increased intracerebral pressure, metabolic acidosis or alkalosis)
  • Standard contraindications for MRI scanning
  • Verbal confirmed pregnancy
  • Anamnesticly a history of neurological disease or current neurological deficits.

Trial design

400 participants in 2 patient groups

Neurosurgical patients
Description:
• Neurosurgical diseases with the potential to alter blood flow to the brain: * Cerebrovascular disease * Brain tumors * Normal Pressure Hydrocephalus
Treatment:
Other: Advanced imaging investigation
Healthy subjects
Description:
* Male and Female subjects \>18 years of age * Written Informed Consent by the participant after information about the project. Foreign speaking healthy subjects should be accompanied by a person with sufficient German language proficiency to act as a translator
Treatment:
Other: Advanced imaging investigation

Trial contacts and locations

1

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Central trial contact

Jorn Fierstra, MD, PhD; Luca Regli, Professor

Data sourced from clinicaltrials.gov

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