Selecting Hypoxic Tumours for Treatment Modification
Launched by UNIVERSITY OF MANCHESTER · Jan 15, 2025
Trial Information
Current as of August 20, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating a new way to improve treatment for patients with bladder and prostate cancer who have what are called "hypoxic tumours." These tumours do not get enough oxygen, making them harder to treat with standard radiotherapy. The researchers have developed a special test that looks at gene activity in tumours to identify which patients have hypoxic tumours. By identifying these patients, doctors can provide more effective treatments, potentially improving outcomes. The goal of the study is to show that this gene test can help predict which patients will benefit from specific treatments designed to enhance the effects of radiotherapy.
To participate in this trial, patients must be at least 18 years old and receiving radiotherapy at the Christie NHS Foundation Trust. They also need to be able to undergo MRI scans and give informed consent to join the study. If eligible, participants can expect to undergo additional imaging and receive tailored treatment based on the results of the gene test. It’s important to note that the trial is currently recruiting participants, and all involved will be closely monitored throughout the process to ensure their safety and the effectiveness of the treatment modifications.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • This will be tumour site dependent.
- Bladder:
- • Older than age 18 years.
- • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
- • Able to give informed consent.
- Cervix:
- • Older than age 18 years.
- • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
- • Able to give informed consent.
- Prostate:
- • Older than age 18 years.
- • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
- • Able to give informed consent.
- Exclusion Criteria:
- • This will be tumour site dependent
- Bladder:
- • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
- • Unable to tolerate MRI scans.
- • Pregnancy.
- Cervix:
- • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
- • Unable to tolerate MRI scans.
- • Pregnancy.
- Prostate:
- • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
- • Unable to tolerate MRI scans
About University Of Manchester
The University of Manchester is a leading research institution known for its commitment to advancing healthcare through innovative clinical trials. With a strong emphasis on multidisciplinary collaboration, the university leverages its extensive expertise in biomedical research and clinical practice to develop and evaluate new therapies and interventions. The institution is dedicated to improving patient outcomes and public health by conducting rigorous, ethically sound trials that adhere to the highest standards of scientific integrity. Through its state-of-the-art facilities and a robust network of healthcare partnerships, the University of Manchester actively contributes to the global body of medical knowledge and the translation of research findings into clinical applications.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Manchester, , United Kingdom
Greater Manchester, , United Kingdom
Patients applied
Trial Officials
Ananya Choudhury, Professor
Principal Investigator
University of Manchester
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported