An interventional trial comparing ferumoxytol and gadolinium for estimating the immune cell content in brain tumours.
- Conditions
- Stage 3 and 4 astrocytomabrain tumour metastasisCancer - Brain
- Registration Number
- ACTRN12622000218796
- Lead Sponsor
- Tania Slatter
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 80
1.Patients with an imaging diagnosis based on the baseline diagnostic MRI scan (gadolinium contrast) of primary stage 3 or 4 astrocytoma, or brain tumour metastasis.
2.No steroid treatment that has been administered to the patients between the time of the baseline diagnostic scan and the ferumoxytol infusion.
1.Patients who are younger than 18 years old.
2.Patients who are pregnant or breast feeding.
3.Patients who have known allergy to iron preparations or other medication allergies.
4.Patients who have haemochromatosis or known clinically significant liver function abnormalities.
5.The initial diagnostic MRI demonstrates intracranial haemorrhage, calcification or other susceptibility blooming artifacts.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method