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Detection of pseudoprogression using CT perfusion in patients with Glioblastoma Multiforme post-treatment

Completed
Conditions
Glioblastoma Multiforme
Cancer
Registration Number
ISRCTN68166254
Lead Sponsor
The Walton Centre NHS Foundation Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
20
Inclusion Criteria

1. Patients with glioblastoma multiforme tumours who will be discussed in the regional neuro-oncology multidisciplinary team meeting
2. Patients exhibiting any tumour progression on their first follow-up imaging immediately after radiotherapy, surgery or chemotherapy post-treatment without clinical progression

Exclusion Criteria

Patients who exhibit tumour progression both clinically (symptoms) and on imaging on the first follow-up imaging immediately following radiotherapy, chemotherapy or surgery following treatment

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnosis of true tumour progression measured by MRI scan 8 weeks after treatment
Secondary Outcome Measures
NameTimeMethod
Better diagnosis and improved treatment options
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