Clinical trial · Interventional
FCI in Post-operative Low Grade Gliomas
Non-invasive In-vivo Characterisation of Postoperative Low Grade Gliomas Using Field Cycling Imaging (FCI)
NCT06294418CI-TRIAL-00108850completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this pilot study is to explore the utility of a new imaging technique, called Field Cycling Imaging (FCI), in postoperative low grade gliomas. The main question it aims to answer is if FCI can differentiate subtypes of low grade gliomas. Participants will have one FCI scan.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Glioma | Glioma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Field Cycling Imaging (FCI) | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Low grade glioma
- description
- Patients with postoperative low grade glioma will undergo one FCI scan.
- interventionNames
- Device: Field Cycling Imaging (FCI)
Primary outcomes (1)
- measure
- Differentiation of sub-types of low grade glioma assessed by Field Cycling Imaging (FCI) T1 dispersion profiles
- timeFrame
- At baseline
- description
- Validation of FCI T1 dispersion profiles as a non-invasive technology to differentiate sub-types of low grade glioma.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 16 Years
Show eligibility criteria text
Inclusion Criteria: * Patients with post operative low-grade glioma. * Capacity to give informed consent. * Capacity to co-operate with the scanning procedures and duration. * Age 16 and above. * Participants who can pass through a 50 cm-diameter circular hoop to ensure they will be able to fit inside the scanner. * Participants who meet the safety criteria for undergoing an MRI scan. * Participants must be mobile enough to be positioned onto the FCI scanner couch. Exclusion Criteria: * MRI-incompatible conditions, as detected in the MRI safety screening form. * Restrictions to mobility that would prevent the correct positioning in the scanner by trained research radiographer (e.g., severe kyphosis). * Participants who are unable to give fully informed consent. * Women who are pregnant. * Participants who are unable to understand or communicate in English. * Patients who suffer from claustrophobia.
References
Publications (0)
Data not yet available
No reference posted for this study.