IMAGO
A single arm exploratory study examining the feasibility of imaging glioblastoma pH using CEST MRI
Full Title
A single arm exploratory study examining the feasibility of imaging glioblastoma pH using CEST MRI
Chief Investigator: Simon Lord
ISRCTN Identifier: ISRCTN86522205
Sponsor: University of Oxford
Study Design
Single arm exploratory
Study Population
Previously untreated glioblastoma patients scheduled for resection or debulking.
Study Status
Closed to Recruitment
Study Schema
Inclusion Criteria
- Participant is willing, capable of cooperating with the protocol and able to give informed consent for participation in the study.
- Male or Female, aged 18 years or above.
- Diagnosed with glioblastoma and scheduled for neurosurgical resection or debulking.
Exclusion Criteria
- Intolerant of MRI brain (for example: claustrophobia).
- MRI brain contraindicated (for example: implanted electric and electronic devices, heart pacemakers, insulin pumps, implanted hearing aids, neuostimulators, intracranial metal clips, metallic bodies in the eye).
- Neoadjuvant chemotherapy/radiotherapy treatment for glioblastoma which would interfere with the interpretation of trial results.
- Pregnancy.
- Other psychological, social or medical condition that the investigator considers would make the patient a poor trial candidate or could interfere with protocol compliance or the interpretation of trial results.
Primary objective
To evaluate CEST contrast image obtained from CEST MRI in glioblastoma
Secondary Objectives
- Explore if measurement of tumour protein levels relates to CEST MRI imaging signal
- Explore if measurement of tumour pH relates to CEST MRI imaging signal
- Explore if hypoxia relates to CEST MRI imaging signal
- Explore if ASL MRI perfusion imaging signal relates to CEST MRI imaging signal
IMAGO Trial Office (OCTO)
General Enquiries:
Tel: +44 (0)1865 617 083
Fax: +44 (0)1865 617 010
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In this section
- About Us
- Work With Us: Careers In Trial Management
- Work With Us: Information for Investigators and Commercial Organisations
- Information for Patients, their Families and Carers
- Patient and Public Involvement & Engagement (PPIE)
- Current Trials
- Trials in Set Up
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Completed Trials
- CHARIOT: M6620 plus standard treatment in oesophageal and other cancer
- LUD 2015-005: ANTI-PD-L1 in combination with chemo(radio)therapy for oesophageal cancer
- SCALOP-2: Systemic therapy and Chemoradiation in Advanced Localised Pancreatic cancer–2
- CYTOFLOC: Cytosponge™ for post‐chemoradiation surveillance of oesophageal cancer
- FRONTIER: Fluciclovine (18F) imaging of breast cancer
- NuTide:301: Safety, pharmacokinetics and clinical activity of NUC-3373, a nucleotide analogue, in participants with advanced solid tumours.
- IMAGO: A single arm exploratory study examining the feasibility of imaging glioblastoma pH using CEST MRI
- TARDOX: Targeted chemotherapy using focused ultrasound for liver tumours
- CAMELLIA: Anti-CD47 antibody terapy in relapsed/refractory Haematological Malignancies
- ATOM: Atovaquone as Tumour HypOxia Modifier
- 6MP: A Phase II Clinical Trial in Patients with BRCA Defective Tumours
- AspECT: A Phase III, Randomised, study of Aspirin and Esomeprazole Chemoprevention in Barrett’s Metaplasia
- BKM120: Palliative thoracic radiotherapy plus BKM120
- CHOP-OR: Study of CHOP with Ofatumumab in Patients with Richter's Syndrome
- NEOPANC-01 - Pre-operative, Window-of-opportunity Study to Assess Gene Expression in Patients With Resectable, Locally Advanced, or Metastatic Pancreatic Cancer
- COG : Gefitinib for oesophageal cancer progressing after chemotherapy
- DATACAP: Dose Adaptation of Capecitabine Using Mobile Phone Toxicity Monitoring
- DEBIOC: Dual Erb B Inhibition in Oesophago-gastric Cancer
- DOC-MEK: A double-blind randomized phase 2 trial of docetaxel with or without selumetinib in wild-type BRAF advanced melanoma
- EnROL: Conventional versus laproscopic surgery for colorectal cancer within an enhanced programme
- FOXFIRE: An open-label randomised phase III trial of 5-Fluorouracil, OXaliplatin and Folinic acid +/- Interventional Radio-Embolisation as first line treatment for patients with unresectable liver-only or liver-predominant metastatic colorectal cancer
- LINES: Eurosarc Trial of Linsitinib in advanced Ewing Sarcoma
- MErCuRIC1: MEK and MET Inhibition in Colorectal Cance
- MPP: Application of mobile phone technology for managing chemotherapy-associated side-effects
- OXO-PCR-01: Oxford Ovarian Cancer Predict Chemotherapy Response 01
- PACMEL: A randomised phase 2 study of paclitaxel with or without GSK1120212 or pazopanib in advanced wt BRAF melanoma
- PemBla: A parallel group phase I/II marker lesion study to assess the safety, tolerability and efficacy of intravenous or intravesical pembrolizumab in intermediate risk recurrent non-muscle invasive bladder cancer
- ART: Anal squamous cell carcinoma: Investigation of functional imaging during chemoRadioTherapy
- RHYTHM-1: Modulation of Radiotherapy according to HYpoxia: exploiting changes in the Tumour Microenvironment to improve outcome in rectal cancer
- RADVAN: A randomised double blind phase 2 trial of whole brain radiotherapy with or without vandetanib in metastatic melanoma with brain metastases.
- SPARC: SBRT pre-operatively for pancreatic cancer
- VICTOR: Post-treatment stage of a Phase III, randomised, double blind, placebo-controlled study of rofecoxib (VIOXX®) in colorectal cancer patients following potentially curative therapy.
- WBRT: Whole Brain Radiotherapy following local treatment of intracranial metastases of melanoma – A randomised Phase III trial.
- QUASAR2: Multicentre international study of capecitabine ± bevacizumab as adjuvant treatment of colorectal cancer
- SONATINA: A Phase II Multi-Centre Randomised Controlled Study Of Nelfinavir Addition to Radiotherapy Treatment In Neo-Adjuvant Therapy for Rectal Cancer.
- SCOT: Short Course Oncology Treatment - A study of adjuvant chemotherapy in colorectal cancer by the CACTUS and OCTO groups.
- PanDox : Feasibility of Enhanced Chemotherapy Delivery to non-resectable Primary Pancreatic Tumours Using Thermosensitive Liposomal Doxorubicin (ThermoDox®) and Focused Ultrasound