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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04715503
Other study ID # T225/2020
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 14, 2021
Est. completion date October 2022

Study information

Verified date January 2021
Source Turku University Hospital
Contact Dan Laukka, MD
Phone +358 2 313 2799
Email dan.laukka@tyks.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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).


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 2022
Est. primary completion date January 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility 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.

Study Design


Intervention

Radiation:
PET imaging, 18F-FDG
PET-MRI with 18F-FDG
PET imaging, 68Ga-DOTANOC
PET-CT with 68Ga-DOTANOC

Locations

Country Name City State
Finland Turku University Hospital Turku

Sponsors (2)

Lead Sponsor Collaborator
Turku University Hospital University of Turku

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary PET-imaging of unruptured intracranial aneurysms Uptake 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)
1 month
Secondary Risk factors for intracranial aneurysm inflammation Uptake of 18F-FDG or 68Ga-DOTANOC and histological findings correlation to aneurysm size and shape, smoking, hypertension, location of aneurysm. 1 month
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