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Analysis of Retrospectively Collected MRI Referral DataAutoProMptNCT07918313

Automated Vetting and Protocolling of MRI Examinations

An observational study of Analysis of Retrospectively Collected MRI Referral Data, run by Edozie Iweka.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Background Vetting and assigning of protocols to MRI scan requests are usually carried out by radiologists and radiographers. This way is both time-consuming and prone to error. Recent improvements in Artificial Intelligence (Al) like Large Language Models (LLMs) are better at processing human language. Read more about this study

Who is it for?
Any age
How many people
900,000 participants
Where
No sites listed yet
Study dates
1 Feb 2027to 28 Sep 2029
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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: This study is multi-stage multi-center research involving retrospective MRI referral data of patients and collected across three NHS Foundation Trusts in the United Kingdom.

Who may be able to join

  • Patients who have had MRI examinations in the study sites
  • Patients with MRI referrals submitted through electronic referral systems
  • Patients whose MRI referrals were vetted and protocolled prior to examination

Who cannot join

  • Patients who have had other imaging examination outside the MRI
  • Patients with paper referrals scanned in electronic referral systems
  • Patients for MRI examinations without vetting and protocolling

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Edozie Iweka, MSc (Dist) contact

+441225386989

eoi29@bath.ac.uk

About this study

Official title: Automated Vetting and Protocoling of MRI Examination Referrals Using Explainable Large Language Models (LLM) With Retrieval Augmented Generation (RAG) (XLLM) Techniques- A Multi-stage Study

Background Vetting and assigning of protocols to MRI scan requests are usually carried out by radiologists and radiographers. This way is both time-consuming and prone to error. Recent improvements in Artificial Intelligence (Al) like Large Language Models (LLMs) are better at processing human language. It could be used to improve tasks like image reporting and assigning protocols in radiology.

Approach Firstly, I will find out about the delays in the way this is currently done. I will use a survey to find out the perceptions of radiologists to both the current process and the proposed Al intervention.

Read more

I will then use an LLM to undertake referral and protocol tasks. I will compare its performance to the performance of clinical specialists and established guidelines.

I will present the explanation reports to radiologists and ask them if they can be understood and whether they can be trusted as clinically reliable.

Impact My research could help reduce the workload and time radiologists spend dealing with scan requests. The findings will help design future research to consider application in real clinical settings.

Being tested
No Intervention: Observational Cohort
Keywords
Artificial Intelligence, Large Language Models, Retrieval Augmented Generation, Magnetic Resonance Imaging (MRI), protocolling, Vetting, Explainability.

What participants receive

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

  • No Intervention: Observational CohortOther

    No Intervention as this is an experiment on retrospective collected referral data

Study groups in NCT07918313
Study groupRoleWhat they receive
GroupAdult Patients undergoing MRI examinations
Receives: Other: No Intervention: Observational Cohort

What is being measured

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

  1. Accuracy

    Accuracy of pretrained LLMs+RAG in automating vetting and protocolling of MRI examination referrals.

    Measured: Through study completion, an average of 2 years

Secondary outcomes (1)
  1. Clinical Usefulness

    Clinical usefulness of explainability reports on the performance of pretrained LLMs+RAG in automating vetting and protocolling of MRI examination referrals.

    Measured: Through study completion, an average of 2 years

Timeline

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

  1. First posted5 Nov 2026
  2. Study start1 Feb 2027 (estimated)
  3. Primary completion1 Apr 2027 (estimated)
  4. Study completion28 Sep 2029 (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
Retrospective
Enrolment
900,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07918313
Sponsor's protocol ID
18376
Acronym
AutoProMpt
Status last verified
Nov 2026
First submitted
28 Oct 2026
Last updated
5 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: No patient identifiable data will be collected from this study. All collected data will be held by the sponsor institution, University of Bath as per local research data policy.

Questions about this trial

What is this clinical trial studying?

An observational study of Analysis of Retrospectively Collected MRI Referral Data, run by Edozie Iweka.

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 3 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: opening soon, as of the sponsor's last update on 5 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

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 Edozie Iweka, MSc (Dist) (+441225386989, eoi29@bath.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Accuracy (time frame: Through study completion, an average of 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 Nov 2026.

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