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Status unknownNCT05285072GaDFOUpdated Mar 17, 2022

Siderophores for Imaging Infection Using 68Ga-DFO

An observational study in Vascular Graft Infection, sponsored by Guy's and St Thomas' NHS Foundation Trust. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-03-17.

Sponsored by Guy's and St Thomas' NHS Foundation Trust · Observational

The sponsor has not verified this record recently (last verified Mar 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

This is a single center pilot study involving a single study visit for participants, with remote follow up data collected at 24 hours. Follow up at 3 months and 6 months later occurs as standard of care.

The purpose of the study is to find out if a new type of imaging tracer (68Ga-DFO) can be used to show infection in patients with vascular grafts using PET/CT scans. These infections may be associated with significant ill health and mortality and can be difficult to diagnose. Effective treatments can require major surgery and long-term antibiotic therapy which may not be well tolerated nor feasible. Development of new imaging tracers that could detect bacteria causing graft infections with PET-CT scanners has great potential to benefit patients being considered for vascular surgery.

A PET-CT scan combines images from a CT (Computerised Tomography) scan and a PET (Positron Emission Tomography) scan. The CT scan takes a series of X-rays across the organs inside the body. The PET scan uses a mildly radioactive tracer to show up areas of activity inside the body. The 68Ga-DFO tracer mimics particles that bacteria make to take up iron from the body to help them grow. The investigators hope this new tracer will go to areas where bacteria are causing infection and tell if the graft is infected. The investigators hope this type of tracer could be a better way to show infection than the tests currently used to diagnose infection.

Read the detailed description

This study is a first in human mechanistic study hypothesizing that siderophore complexes labelled with a radiotracer (Gallium-68) will be taken up in sites of infection in patients with a vascular graft.

Study objectives are to:

i) Determine if siderophore uptake occurs in sites of infection using the radiolabelled siderophore 68Ga-DFO in patients with a vascular graft on PET/CT scans.

ii) Determine if siderophore uptake as measured by the radiolabelled siderophore 68Ga-DFO is specific for infection by exploring whether uptake occurs in individuals with vascular grafts without infection and by characterising the uptake in normal tissues.

The injected substances are well-known licensed products.

The study will involve performing 68Ga-DFO PET/CT scans in 30 patients with vascular grafts, including 25 patients with diagnosed infection according to current syndromic criteria and 5 patients with a vascular graft but no evidence of any infection. Patients with infection will be recruited from patients who have had a prior FDG-PET-CT scan performed as part of their routine care which shows suspected graft infection.

All patients will have 'static' PET-CT scans following injection of the tracer. The scans will take 30 minutes.

The first ten patients with graft infection will also have 'dynamic' scans performed immediately after tracer injection lasting for 90 minutes. The result of these scans (e.g. time activity curves) will inform the scan protocol of the subsequent patients (e.g. uptake time). Up to 10 of these patients will have venous blood sampling at 8 time points up to 120 minutes after injection.

Patients will be followed up in person or by telephone 24 hours after the scan. Apart from this no specific follow up procedure outside standard of care is planned within this study.

02

Conditions studied

  • Vascular Graft Infection

Keywords

  • positron emission tomography
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's planned enrollment of 30 is below the median of 240 across 2,136 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Guy's and St Thomas' NHS Foundation Trust is the lead sponsor of 284 studies on the registry; 79 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Cohort 1 Patients attending the Department of Vascular Surgery or the PET Centre (after referral for a PET scan with the indication of suspected or diagnosed vascular graft infection) at Guy's \& St. Thomas' Hospitals in London.

Cohort 2 Patients with no evidence of vascular graft infection attending a routine follow-up visit after surgery in the Department of Vascular Surgery at Guy's \& St. Thomas' Hospitals . Patients will have a blood sample prior to imaging to ensure that CRP is ≤5.

Inclusion criteria

  • Age 18 and older
  • Women of childbearing potential must have documented negative pregnancy test prior to tracer administration.
  • Willing and able to give informed consent
  • Able to comply with the PET imaging protocol
  • Patients with vascular grafts in situ
  • Positive FDG-PET/CT in the case of patients with suspected or diagnosed graft infections

Exclusion criteria

Exclusion Criteria:

  • Aged under 18
  • Pregnancy or lactation
  • Prisoners
  • Any lack of capacity to consent, including lack of adequate understanding of written or spoken English.
  • Iron infusion within 1 week of 68Ga-DFO PET/CT scan (can potentially hamper the sensitivity of DFO by decreasing the number of siderophore receptors in the bacteria).
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Vascular graft infection

    Patients with confirmed vascular graft infection according to current syndromic criteria.

    Radiation: PET-CT scan

  • Vascular graft without infection

    Patients with no clinical evidence of infection and CRP less than 5.

    Radiation: PET-CT scan

Interventions

  • RadiationPET-CT scan

    PET-CT scan using 68Ga-DFO

06

What researchers measure

Primary outcomes

  1. siderophore uptake

    Observe level of siderophore uptake around vascular graft in patients with known infection and in patients without infection

    Time frame: baseline

Secondary outcomes

  1. Infective agents associated with a confirmed vascular graft infection

    from blood cultures or organisms recovered from an explanted graft, intra-operative specimen, from percutaneous or radiologically guided aspirate of peri-graft fluid

    Time frame: 6 months post baseline

Other outcomes

  1. Infection diagnosis

    Details will be collected of any evidence of vascular graft infection from blood cultures or organisms recovered from an explanted graft, intra-operative specimen, from percutaneous or radiologically guided aspirate of peri-graft fluid and therapy received.

    Time frame: 6 months post baseline

07

Study locations

1 of 1 sites recruiting
  • Kings College London and Guy's and St Thomas' Hospital PET Centre
    London, SE1 7EH, United Kingdom
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05285072
Lead sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
King's College London
Responsible party
Sponsor
First posted
Mar 17, 2022
Start date
Mar 15, 2022 (estimated)
Primary completion
Jul 31, 2023 (estimated)
Completion
Jan 31, 2024 (estimated)
Last update
Mar 17, 2022

Study contacts

Sally F Barrington, MD
Contact
sally.barrington@kcl.ac.uk
02071884988
Sally Barrington, MD
principal investigator · King's College London

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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