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AzTrials

Cerebral Small Vessel DiseasePUFFINS BHNCT06947876

PUFFINS Brain Health Study

An observational study of Cerebral Small Vessel Disease, run by University of Aberdeen at 2 sites in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Small vessel disease (SVD) is a major cause of stroke and contributor to dementia cases. As work continues to develop new treatments to address the impact of SVD, new imaging techniques are needed to identify and track the progression of brain changes that occur with SVD. Read more about this study

Who is it for?
Ages 50 years and older
Conditions the study is for
Cerebral Small Vessel Disease
What is being tested?
Enrolment 3T MRI research scan, Enrolment Field-cycling Imaging research scan and Enrolment ultra-low field MRI research scan
Type of treatment
Pill or oral medicine
How many people
85 participants
Where
2 sitesUnited Kingdom
Study dates
17 Dec 2025to May 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Participants who small vessel disease, Fazekas score 1 to 3. Study population will be recruited from the NHS Grampian region.

Who may be able to join

  • Adults ≥ 50 years old.
  • Subjects who do not report problems with memory.
  • Small vessel disease (Fazekas score 1 to 3).
  • Suitable body habitus.
  • Able to understand written and spoken English.

Who cannot join

  • History of major stroke (minor stroke/Transient Ischaemic Attacks or lacunar stroke are acceptable).
  • Individuals unable to give informed consent.
  • Contra-indications to MRI scanning such as implantable cardiac devices.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Mary Joan MacLeod contact

+44 1224 438352

m.j.macleod@abdn.ac.uk

Gordon D Waiter contact

+44 1224 438356

g.waiter@abdn.ac.uk

United Kingdom2 sites, 2 recruiting
  • Aberdeen Biomedical Imaging Centre, University of Aberdeen

    Aberdeen, AB24 3FX

    Gordon Waiter, PhD, +44 1224 438356, g.waiter@abdn.ac.uk

    Mary Joan MacLeod, PhD, +44 1224 437842, m.j.macleod@abdn.ac.uk

    Recruiting
  • AMT Center, Univeristy of Aberdeen

    Aberdeen, AB24 3FX

    Mathieu Sarracanie, PhD, +44 1224 437365, mathieu.sarracanie@abdn.ac.uk

    Najat Salameh, PhD, +44 1224 437360, najat.salameh@abdn.ac.uk

    Recruiting

Other trials in United Kingdom

About this study

Official title: Proving the Utility of Ultra-low Field MRI for Assessing Brain Health

Small vessel disease (SVD) is a major cause of stroke and contributor to dementia cases. As work continues to develop new treatments to address the impact of SVD, new imaging techniques are needed to identify and track the progression of brain changes that occur with SVD. Magnetic Resonance Imaging (MRI) is the gold standard to diagnose poor brain health due to small vessel disease. However, current MRI systems are expensive and complex to operate, and so access is limited.

Low-field MRI technology, operating at magnetic field strengths many times lower than conventional MRI, can make brain imaging much more cost-effective and accessible. However, further work is needed to develop low-field MRI towards clinically feasible assessments of brain health. The University of Aberdeen hosts a unique network of researchers and imaging technologies that is now making it possible to test and develop different low-field MRI approaches towards solving key healthcare challenges.

The aim of this study is to evaluate the potential of two distinct approaches, field-cycling imaging (FCI) and ultra-low field MRI (ULF-MRI), to detect brain changes linked with small vessel disease. Automated methods will be developed to analyse images and extract measurements that detect and track progression of disease severity.

Read the detailed description

Cerebral small vessel disease (SVD) is a major underlying contributor to ischaemic and haemorrhagic stroke, cognitive decline, and dementia. Neuroimaging features of SVD have been shown to be associated with increased risk of stroke occurrence, reoccurrence, and cognitive decline post-stroke. New approaches are needed that target SVD diagnosis, monitoring, and treatment, to improve outcomes across the stroke and cognitive decline care pathways. However, providing equitable access to advanced medical technologies across the Scottish population is becoming a significant burden on the NHS and wider clinical community. Low-field MRI, which is both more cost-effective and less complex to operate, has the potential to address this growing societal burden at a whole-population level. Whilst on-going research efforts remain focussed on developing new interventions to slow progression of SVD and improve treatment outcomes, work is also needed to improve approaches to assess SVD pathophysiology, severity, progression, and treatment outcome. Repeated assessment with magnetic resonance imaging (MRI), is recognised as the best solution to detect the multiple features that combine to produce SVD. This has the potential to identify markers of stroke risk and cognitive decline and, in future, guide tailored treatments to better manage stroke risk and improve post-stroke long-term outcomes. No other imaging technique, blood test or other assessment can provide the necessary information. However, the high cost and infrastructure demands of conventional MRI means that while it is feasible for clinical trials and research, it cannot realistically be used for widespread repeated brain imaging assessment, or screening, for SVD. For this reason, robust and reliable imaging methods that can be easily implemented across the whole Scottish population, rural/urban, wealthy/deprived must be developed. Operating at magnetic field strengths up to 10,000 times lower than conventional MRI, low-field MRI technologies provide a unique opportunity to make repeated brain imaging cost-effective and accessible in community and outpatient settings. The utility of commercially available portable low-field MRI technology, operating at a fixed field of 64 mT (milliTesla), has already been proven for imaging acute stroke at the bedside of patients and recent preliminary findings have indicated its feasibility to detect moderate and severe SVD. However, the novelty of portable low-field MRI means that its full potential has yet to be realised, and work is now required to develop low-field quantitative imaging approaches to enhance the capabilities of low-field MRI to extract underlying features related to brain health and SVD severity. We aim to provide a stepping-stone to optimised fixed low-field MRI technology by leveraging the unique capabilities of field-cycling imaging (FCI), a unique whole-body MRI technology developed at the University of Aberdeen. IRAS Form Reference: 25/PR/0216 IRAS Version 6.4.1 Date: 13/02/2025 350553/1711955/37/104 7Investigations using field-cycling technologies, which vary the strength of the magnetic field during acquisition, have shown unique sensitivity to tissue features and contrast mechanisms that are invisible at higher, fixed, magnetic fields such as 1.5 and 3T. Furthermore, using FCI, differences between healthy tissue and stroke pathology have been observed. Our own preliminary results, using the mark 2 FCI scanner to image patients with SVD at field strengths between 0.2 and 200 mT have shown a significant positive linear correlation between the volume of SVD extracted from FCI images and from 3T MRI images. However, these preliminary results, limited to a single slice acquisition at 3.1 x 3.1 x 10 mm resolution, do not provide the full evidence needed to design new, cost-effective and accessible, lowfield MRI scanners that would enable widespread, repeated brain imaging assessment for SVD. The objective of this proposal is therefore to address this evidence gap and to inform the design of new low-field MRI technologies tailored to extracting key markers of SVD. First, by utilising the unique capabilities of the new mark 3 FCI scanner, now onsite at Aberdeen Royal Infirmary, imaging data will be acquired at multiple different field strengths, and a higher pixel resolution. This data will be used to determine the most effective low-field approach to identify markers of SVD (e.g., white matter changes, reduced perfusion, microbleeds, recent lacunar infarcts) and SVD progression. Second, by acquiring imaging data from both field-cycling imaging (FCI) and a separate fixed low-field MRI scanner, the extent of agreement between assessments of SVD will be examined.

Being tested
Enrolment 3T MRI research scan, Enrolment Field-cycling Imaging research scan, Enrolment ultra-low field MRI research scan, Follow up 3T MRI research scan, Follow up Field-cycling Imaging research scan
Keywords
Field-cycling imaging, Ultra-low field MRI
Medical subject headings
Cerebral Small Vessel Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Enrolment 3T MRI research scanOther

    Enrolment research scan performed with 3T magnetic resonance imaging scanner.

  • Enrolment Field-cycling Imaging research scanOther

    Enrolment research scan performed with Field-Cycling Imaging scanner.

  • Enrolment ultra-low field MRI research scanOther

    Enrolment research scan performed with ultra-low field MRI scanner

  • Follow up 3T MRI research scanOther

    Follow up research scan performed with 3T magnetic resonance imaging scanner, 18-months after baseline scans.

  • Follow up Field-cycling Imaging research scanOther

    Follow up research scan performed with Field-Cycling Imaging scanner, 18-months after baseline scans.

  • Follow up ultra-low field MRI research scanOther

    Follow up research scan performed with Ultra-low field MRI scanner, 18-months after baseline scans.

  • Enrolment cognitive assessment interviewOther

    Enrolment interview performed to complete cognitive assessment scoring of Montreal Cognitive Assessment, EQ-5D, Trail making test, Animal naming test, controlled oral word association test, and Hopkins Verbal Learning Test.

  • Follow up cognitive assessment interviewOther

    Follow up interview performed to complete cognitive assessment scoring of Montreal Cognitive Assessment, EQ-5D, Trail making test, Animal naming test, controlled oral word association test, and Hopkins Verbal Learning Test. Performed 18-months after baseline interview.

Study groups in NCT06947876
Study groupRoleWhat they receive
Participants with mild small vessel disease (Fazekas score = 1)Participants with mild small vessel disease, defined by a Fazekas score of 1.
Receives: Other: Enrolment 3T MRI research scan; Other: Enrolment Field-cycling Imaging research scan; Other: Enrolment cognitive assessment interview
Participants with moderate small vessel disease (Fazekas score = 2)Participants with mild small vessel disease, defined by a Fazekas score of 2.
Receives: Other: Enrolment 3T MRI research scan; Other: Enrolment Field-cycling Imaging research scan; Other: Enrolment cognitive assessment interview
Participants with severe small vessel disease (Fazekas score = 3)Participants with mild small vessel disease, defined by a Fazekas score of 3.
Receives: Other: Enrolment 3T MRI research scan; Other: Enrolment Field-cycling Imaging research scan; Other: Enrolment cognitive assessment interview
Follow up group. Participants with moderate or severe small vessel disease (Fazekas score = 2 or 3).Participants with moderate or severe SVD (deep white matter Fazekas 2 or 3) who will undergo an extra low-field MRI scan and will have a follow up visit at 18 months.
Receives: Other: Enrolment 3T MRI research scan; Other: Enrolment Field-cycling Imaging research scan; Other: Enrolment ultra-low field MRI research scan; Other: Follow up 3T MRI research scan; Other: Follow up Field-cycling Imaging research scan; Other: Follow up ultra-low field MRI research scan; Other: Enrolment cognitive assessment interview; Other: Follow up cognitive assessment interview

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Small vessel disease volume agreement between enrolment Field-Cycling Imaging and enrolment 3T MRI.

    Linear regression analysis will be performed between small vessel disease volume obtained from Field-Cycling Imaging (FCI) and 3T MRI.

    Sensitivity will be determined as the effect gradient (gradient of the line of best fit between FCI volume and 3T MRI volume). Precision will be determined as coefficient of variation. Agreement will be determined as Dice coefficient.

    Measured: At enrolment

  2. Small vessel disease volume agreement between follow up Field-Cycling Imaging and follow up 3T MRI.

    Linear regression analysis will be performed between small vessel disease volume obtained from Field-Cycling Imaging (FCI) and 3T MRI.

    Sensitivity will be determined as the effect gradient (gradient of the line of best fit between FCI volume and 3T MRI volume). Precision will be determined as coefficient of variation. Agreement will be determined as Dice coefficient.

    Measured: At 18 month follow up

Secondary outcomes (4)
  1. Small vessel disease volume agreement between enrolment Field-Cycling Imaging and enrolment Ultra-low Field MRI.

    Linear regression analysis will be performed between small vessel disease volume obtained from Field-Cycling Imaging (FCI) and Ultra-low Field MRI.

    Sensitivity will be determined as the effect gradient (gradient of the line of best fit between FCI volume and Ultra-low Field MRI volume). Precision will be determined as coefficient of variation. Agreement will be determined as Dice coefficient.

    Measured: At enrolment

  2. Small vessel disease volume agreement between follow up Field-Cycling Imaging and follow up Ultra-low Field MRI.

    Linear regression analysis will be performed between small vessel disease volume obtained from Field-Cycling Imaging (FCI) and Ultra-low Field MRI.

    Sensitivity will be determined as the effect gradient (gradient of the line of best fit between FCI volume and Ultra-low Field MRI volume). Precision will be determined as coefficient of variation. Agreement will be determined as Dice coefficient.

    Measured: At 18 month follow up

  3. Strength of association between small vessel disease volume obtained from Field-Cycling Imaging, with small vessel disease severity (Fazekas score), age, mood, and cognition.

    Linear regression analysis will be performed to assess the strength of associations between small vessel disease volume obtained from Field-Cycling Imaging and small vessel disease severity (Fazekas score), age, mood and cognition derived from the memory, language, and processing speed measures.

    Measured: At enrolment

  4. Strength of association between small vessel disease volume obtained from Ultra-low Field MRI, with small vessel disease severity (Fazekas score), age, mood, and cognition.

    Linear regression analysis will be performed to assess the strength of associations between small vessel disease volume obtained from ultra-low field MRI and small vessel disease severity (Fazekas score), age, mood and cognition derived from the memory, language, and processing speed measures.

    Measured: At 18 month follow up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Apr 2025
  2. Study start17 Dec 2025
  3. Primary completionMay 2027 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
85 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06947876
Sponsor's protocol ID
2-079-24
Other IDs
25/YH/0053
Acronym
PUFFINS BH
Status last verified
Jun 2025
First submitted
1 Apr 2025
Last updated
5 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Senn N, Ross PJ, Ayde R, Mallikourti V, Krishna A, James C, de Vries CF, Broche LM, Waiter GD, MacLeod MJ. Field-cycling imaging yields repeatable brain R1 dispersion measurement at fields strengths below 0.2 Tesla with optimal fitting routine. MAGMA. 2025 Jul;38(3):465-474. doi: 10.1007/s10334-025-01230-w. Epub 2025 Feb 15.

    PubMed 39955477

Questions about this trial

What is this clinical trial studying?

An observational study of Cerebral Small Vessel Disease, run by University of Aberdeen at 2 sites in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Mary Joan MacLeod (+44 1224 438352, m.j.macleod@abdn.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Small vessel disease volume agreement between enrolment Field-Cycling Imaging and enrolment 3T MRI. (time frame: At enrolment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06947876, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.

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