New PET scan method could rival standard test for brain blood flow
NCT ID NCT06584747
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a PET scan can measure brain blood vessel response to a drug called acetazolamide as well as the standard scintigraphy method. Nineteen adults with narrowed brain arteries will undergo both scans. The goal is to see if the newer PET approach is a reliable alternative for diagnosing blood flow problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acetazolamide (Diamox)
- What this could lead to
- If successful, PET scans could replace the older method for assessing brain blood flow, offering a more accessible or detailed diagnostic option.
- What could go wrong
- This is a small, early-phase diagnostic study with only 19 participants. The PET method may not prove as accurate as the standard test, and results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
19 people
The number who actually took part.
- Started
-
Jan 2025
- Expected to finish
-
Apr 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Chronic stenosing cerebral vascular pathology (stenosis \> 70% on Doppler examination or angiography). * Patient aged over 18 years. * Patient who has voluntarily agreed to participate in the study and has signed the written informed consent. * Patient affiliated with a social security system. Exclusion Criteria: * Patient with stenosis less than 70% on Doppler examination or angiography. * Patient with a contraindication to 18F-FDG PET examinations: severe claustrophobia, poorly controlled diabetes during 18F-FDG PET examinations (fasting capillary blood glucose ≥ 11 mmol/L). * Patient with a contraindication to scintigraphy. * Patient with an allergy to sulfonamides (Acetazolamide DIAMOX®). * Patient enrolled in another clinical study with a specified exclusion period. * Minor patient. * Patient unable to give informed consent. * Vulnerable individuals
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Centre Antoine Lacassagne
Nice, 06000, France
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