We'd like your feedback
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
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.
Lorna Smith
+44 0203 437 6647
soprano-icrctsu@icr.ac.uk
Laura Moretti
+44 0208 722 4153
soprano-icrctsu@icr.ac.uk
Ovarian Neoplasms Carcinoma, Ovarian Epithelial
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.
SOPRANO is a multi-centre, randomised phase II trial which aims to assess the impact of Stereotactic radiotherapy (SBRT) and continuing treatment with a PARP inhibitor (PARPi) for patients with oligometastatic or oligoprogressive ovarian, fallopian tube and primary peritoneal carcinoma. SOPRANO will also establish the feasibility and acceptability of delivering SBRT in this setting.
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:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Lorna Smith
+44 0203 437 6647
soprano-icrctsu@icr.ac.uk
Laura Moretti
+44 0208 722 4153
soprano-icrctsu@icr.ac.uk
The study is sponsored by Institute of Cancer Research, United Kingdom and is in collaboration with Royal Marsden NHS Foundation Trust.
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.