ISABELLA: InveStigAting Bladder fiELd-cycLing imAging

Sponsor
University of Aberdeen (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05846165
Collaborator
NHS Grampian (Other)
10
1
10

Study Details

Study Description

Brief Summary

The goal of this pilot study is explore the parameters that can be obtained in bladder tumours by Field-Cycling Imaging (FCI) in patients with both muscle-invasive and non-muscle invasive tumours. The main question it aims to answer is if FCI can give more diagnostic information than conventional tests.

Participants will have one FCI scan and the results will be correlated with the results of CT urogram or CT scan.

Condition or Disease Intervention/Treatment Phase
  • Device: Field-Cycling Imaging (FCI)
N/A

Detailed Description

Patients with organ-confined muscle invasive bladder cancer are treated either by removal of their bladder at cystectomy or by organ-preserving treatment, generally following neoadjuvant chemotherapy. In some cases, the neoadjuvant chemotherapy can shrink the tumour so that it is clinically undetectable but there may still be tumour cells present microscopically. This presents a difficulty during planning of radiotherapy treatments, which could then miss the tumour and lead to tumour recurrence.

Field-Cycling Imaging (FCI) is an emerging imaging technology pioneered at the University of Aberdeen. FCI can image human tissues non-invasively over a wide range of magnetic field strengths, directly informing on multi-scale tissue structure from nanometres to micrometres. FCI has already shown significant potential for enhanced diagnosis in a range of diseases, and recent results show several potential biomarkers of cancer in breast, colon, and brain.

FCI has not been used in bladder cancer before. In this proof-of-concept study, we will recruit patients with both muscle-invasive and non-muscle invasive tumours to explore the parameters that can be obtained in bladder tumours by FCI. Results of the FCI scans will be correlated with the results of CT urogram or CT scan.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
InveStigAting Bladder fiELd-cycLing imAging (ISABELLA)
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Bladder tumours

Participants with muscle-invasive and non-muscle invasive bladder tumours of at least 3 cm in diameter will undergo one FCI scan.

Device: Field-Cycling Imaging (FCI)
FCI scan

Outcome Measures

Primary Outcome Measures

  1. Identification of bladder tumours by Field-Cycling Imaging (FCI) scan [At baseline]

    Validation of FCI T1 dispersion profiles as a non-invasive technology able to detect bladder tumours.

Secondary Outcome Measures

  1. Differentiation of bladder tumours assessed by Field-Cycling Imaging (FCI) T1 dispersion profiles [At baseline]

    Validation of FCI T1 dispersion profiles as a clinical tool for distinguishing non-muscle invasive from muscle-invasive bladder tumours.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients attending for flexible cystoscopy found to have a tumour of at least 3 cm in diameter (muscle-invasive or non-muscle invasive)

  • Participants must be aged 18 and above

  • Participants who meet the safety criteria for undergoing an MRI scan

  • Participants who are able to fit inside the scanner

  • Participants must be able to give fully informed consent

  • Participants must be mobile enough to be positioned onto the FCI scanner couch

Exclusion Criteria:
  • Patients with total hip replacement

  • MRI-incompatible conditions, as detected in the MRI safety screening sheet

  • Participants under 18 years old

  • Participants who are unable to communicate in English

  • Participants who are unable to give fully informed consent

  • Women who are pregnant

  • Restrictions to mobility that would prevent the correct positioning in the scanner

  • Participants who suffer from claustrophobia

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Aberdeen
  • NHS Grampian

Investigators

  • Study Chair: Anne Kiltie, Prof, University of Aberdeen

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Aberdeen
ClinicalTrials.gov Identifier:
NCT05846165
Other Study ID Numbers:
  • 2-115-22
First Posted:
May 6, 2023
Last Update Posted:
May 6, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Aberdeen
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2023