Skip to content

PET-imaging of Unruptured Intracranial Aneurysm Inflammation

PET-imaging of Unruptured Intracranial Aneurysm Inflammation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04715503
Acronym
PET-IA
Enrollment
20
Registered
2021-01-20
Start date
2021-01-14
Completion date
2022-10-31
Last updated
2021-01-20

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

Conditions

Cerebral Aneurysm, Inflammation, Intracranial Aneurysm

Keywords

intracranial aneurysm, PET, inflammation, positron emission tomography, rupture risk

Brief summary

The main purpose of this study is to determine if PET-imaging can be used to evaluate inflammation level of intracranial aneurysms, thus helping to evaluate the rupture risk of intracranial aneurysm.

Detailed description

Study subjects are patients who are diagnosed with an unruptured saccular intracranial aneurysm and planned for elective surgical treatment of intracranial aneurysms. Prior the planned surgery, all study subjects will undergo PET-imaging of the brain with 18F-FDG- and 68Ga-DOTANOC-tracers targeting glucose metabolism and somatostatin receptors in inflammatory cells. After PET-imaging, samples for histopathological examination from the intracranial aneurysm sac will be collected during the surgery from every study subject. Blood samples are collected prior to aneurysm operation from the routine pre-operative laboratory tests. Cerebrospinal fluid samples are collected during the surgical procedure from the surgical site. From blood samples we will evaluate expression of 20 different circulating microRNAs (miRNA) and the level of tumor necrosis factor-1, interleukin 1 beta, vascular endothelial growth factor, and evaluate correlations between miRNA expression and SUVmax in PET-imaging and miRNA and aneurysm histological findings. Correlation between inflammatory findings in histological studies and PET-imaging will be evaluated (correlation of SUVmax to aneurysm histological findings).

Interventions

RADIATIONPET imaging, 18F-FDG

PET-MRI with 18F-FDG

RADIATIONPET imaging, 68Ga-DOTANOC

PET-CT with 68Ga-DOTANOC

Sponsors

University of Turku
CollaboratorOTHER
Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Fusiform intracranial aneurysms * Following medications: Asetylsalisylic acid or non-steroidal anti-inflammatory drugs. * Patients who have contraindication for magnetic resonance imaging (Pace Makers, foreign ferromagnetic bodies or implants) * Patients who are allergic to contrast agents. * Pregnancy * Underage persons * Patients on somatostatin analogue medication or with known neuroendocrine tumor

Exclusion criteria

* Patients who are diagnosed with unruptured intracranial aneurysm with MRI/MRA or DSA * Patients who are planned to undergo surgical treatment (ligation) of the intracranial aneurysm * Age ≥18 and \<75 years. * Saccular intracranial aneurysm with maximum diameter ≥ 3 mm.

Design outcomes

Primary

MeasureTime frameDescription
PET-imaging of unruptured intracranial aneurysms1 monthUptake of 18F-FDG or 68Ga-DOTANOC in intracranial arterial aneurysms as compared to contra-lateral normal vessel as SUVmax or TBR. Correlation of uptake of 18F-FDG or 68Ga-DOTANOC (SUVmax or TBR) to aneurysm histological findings (CD45, CD3, CD5, CD20, CD138 and CD68, SSTR2, SSTR3 and SSTR5)

Secondary

MeasureTime frameDescription
Risk factors for intracranial aneurysm inflammation1 monthUptake of 18F-FDG or 68Ga-DOTANOC and histological findings correlation to aneurysm size and shape, smoking, hypertension, location of aneurysm.

Countries

Finland

Contacts

Primary ContactDan Laukka, MD
dan.laukka@tyks.fi+358 2 313 2799

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026