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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Dr
Marta
Wylot
+44 (0)1223 767062
marta.wylot@nhs.net
Prof
Ferdia
Gallagher
+44 (0)1223 767062
ferdia.gallagher@nhs.net
Ms
Maria
Zamora
-
maria.zamoramorales@nhs.net
Healthy volunteers and healthy patients with known specific genotypes
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
Background and study aims
Magnetic Resonance Imaging (or MRI) plays an important role in detecting, diagnosing, and monitoring different diseases in the body. We often use contrast-enhanced MRI, which enhances and improves the quality of the MRI images. This type of MRI involves an injection of a chemical substance often called gadolinium-based contrast agent.
In this study we aim to develop novel imaging methods for cancer diagnostics and treatment monitoring. When developing a new method, we need healthy volunteers to help define the limits of "normal." Similarly, it is useful to know what the images look like in healthy patients, i.e. patient with a known genetic predisposition to cancer but without manifested cancer. Healthy volunteers and healthy patients are given the same procedure that the patient group receives. Investigators learn about the disease process by comparing the healthy volunteers’ and healthy patients’ images to the cancer patients’ images.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
The presence of any of the following will preclude participation as determined by the delegated investigator:1. Contraindication or inability to tolerate MRI 2. Pregnant or actively breastfeeding woman3. If using an intrauterine contraceptive device (IUCD) as a method of contraception the device should be MRI-safe at 3 T (researcher to confirm)4. Clinically significant cardiac, pulmonary or neurological diseases as determined by the investigators5. Laboratory abnormalities that may impact the study results although no screening will be required for entry into the study.6. Any other significant medical or psychiatric history rendering the subject ineligible as deemed by the investigators
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Prof
Ferdia
Gallagher
+44 (0)1223 767062
ferdia.gallagher@nhs.net
Ms
Maria
Zamora
-
maria.zamoramorales@nhs.net
Dr
Marta
Wylot
+44 (0)1223 767062
marta.wylot@nhs.net
The study is sponsored by Cambridge University Hospitals NHS Foundation Trust and funded by Cancer Research UK Cambridge Institute, University of Cambridge.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.