Skip to content

Dual Perfusion Imaging for Characterizing Vascular Architecture of Brain Lesions

Combined Spin- and Gradient-Echo Perfusion Weighted Imaging for Characterizing Vascular Architecture of Brain Lesions

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05358340
Enrollment
100
Registered
2022-05-03
Start date
2021-09-24
Completion date
2024-08-31
Last updated
2023-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Metastases, Brain Tumor

Brief summary

The objectives of the study are (1) to evaluate the feasibility of using a combined spin- and gradient- echo (SAGE) sequence in dynamic susceptibility contrast magnetic resonance imaging (DSC MRI) and (2) to determine quantitative estimates of vessel density and size to differentiate between areas of radiation necrosis and tumor recurrence.

Interventions

DIAGNOSTIC_TESTDynamic susceptibility contrast magnetic resonance imaging (DSC MRI)

A dye, known as a contrast agent, will be injected through a needle that is inserted into a vein in the arm or hand. Subsequent magnetic resonance imaging will follow.

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with a brain metastasis or primary brain tumour and who will undergo MRI with contrast.

Exclusion criteria

* Subject or subject's legally authorized representative is unable or unwilling to consent to the study. * Subject with documented contrast medium injection contraindication due to severe kidney disease or allergy.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of perfusion parameter: vessel size index (VSI)Baseline to end of study (up to 2 years)Measurements of vessel size index (VSI) will be calculated.
Measurement of perfusion parameter: cerebral blood volume (CBV)Baseline to end of study (up to 2 years)Measurements of cerebral blood volume (CBV) will be calculated.

Countries

Canada

Contacts

Primary ContactAngelica Manalac
dual.perfusion@gmail.com4166035800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026