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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.
Malignant neoplasms of respiratory and intrathoracic organs
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.
We wish to collect CT scan images and clinical data from patients with incidental lung nodules across the London Cancer Alliances. These data would allow computer based assessment of scan images, termed 'radiomics', to develop tools to predict the risk of lung cancer. Such tools could help us decide which patients require further investigation, with serial scans or lung biopsies, and improve early diagnosis rates and therefore patient outcomes.
This study will use data which has been routinely collected as part of normal patient care.
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:
Observational type: Cohort study;
You can take part if:
You may not be able to take part if:
• Absence of at least one technically adequate CT thorax imaging series (defined by visual inspection of presence of imaging data of the thorax in the DICOM record). • Slice thickness > 2.5mm. • Imaging > 10 years old. • Ground truth unknown.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
The study is sponsored by THE ROYAL MARSDEN NHS FOUNDATION TRUST and funded by NHS ENGLAND; THE ROYAL MARSDEN CANCER CHARITY; .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 46118
You can print or share the study information with your GP/healthcare provider or contact the research team directly.