Actively Recruiting

Phase Not Applicable
Age: 35Years +
All Genders
NCT06136611

Preoperative Preradiotherapy TTFields

Led by The Christie NHS Foundation Trust · Updated on 2026-05-08

42

Participants Needed

1

Research Sites

105 weeks

Total Duration

On this page

Sponsors

T

The Christie NHS Foundation Trust

Lead Sponsor

U

University of Manchester

Collaborating Sponsor

AI-Summary

What this Trial Is About

PreOperative PreRAdIotherapy Tumour Treating Fields (PORTRAIT) is a Phase I study that will test the safety and feasibility of Optune administered preoperatively and preradiotherapy in patients with a new radiological diagnosis of glioblastoma (GBM). Participants will be required to undergo additional MRI sequencing scans and provide blood, tear fluid and tissue samples over a maximum of 6 months. After the study patients will follow their standard treatment pathway.

CONDITIONS

Official Title

Preoperative Preradiotherapy TTFields

Who Can Participate

Age: 35Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient is aged >35 years
  • Patient is male or female
  • Patient has a new radiological diagnosis of glioblastoma
  • Patient has a performance status judged by WHO, ECOG score 0-1
  • Patient has been reviewed by Neuro-oncology MDT with consensus that study entry is clinically appropriate and safe
  • Principal Investigator has confirmed study entry is clinically appropriate and safe
  • Intention to treat with surgical resection and postoperative adjuvant therapy as per standard of care
  • Adequate hematological and biochemical parameters for surgery and contrast agent administration
  • Patient has mental capacity to consent
  • Patient is able and willing to give informed consent
  • Patient is able and willing to comply with continuous head shaving
  • Patient is able and willing to wear Optune equipment for the required duration
Not Eligible

You will not qualify if you...

  • Patients with uncontrolled seizures
  • Patients planned for biopsy procedure only
  • Patients suspected of other tumors or known malignancy except non-melanoma skin cancer or certain prostate cancers within past 3 years
  • Patients with contraindications to contrast-enhanced MRI (e.g., claustrophobia, gadolinium allergy)

AI-Screening

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Trial Site Locations

Total: 1 location

1

The Christie NHS Foundation Trust

Manchester, United Kingdom, M204BX

Actively Recruiting

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Research Team

G

Gerben R Borst, MD PhD

CONTACT

M

Melanie Oddy

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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