Prognostic and Diagnostic Added Value of Medical Imaging in Gynecological Cancer (PRODIGYN)
Launched by REGION VÄSTERBOTTEN · May 2, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The PRODIGYN trial is a study that aims to understand how advanced medical imaging can help doctors better diagnose and treat women with cervical, endometrial, and ovarian cancers. Specifically, the researchers want to find out if these imaging techniques can help predict how long patients might live, improve the planning of radiation treatments, and show connections between imaging results and specific markers found in tumor tissue.
Women aged 18 and older who have not yet started treatment for these types of cancer may be eligible to participate. If you join the trial, you will undergo four extra imaging tests in addition to the usual check-ups. These tests will take place at the start of the study and again after three months. The study will follow your health for five years to gather important information. This research is currently looking for participants, so if you fit the criteria, you could help contribute to important findings that may benefit future patients.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Previously untreated primary cervical, endometrial, or strongly suspected epithelial ovarian cancer.
- • Known clinical FIGO stage.
- • \>18 years old.
- • No other known current or previous malignancy within the last 10 years.
- Exclusion Criteria:
- • Imaging findings suggestive of other primary malignancy.
- • Previously included suspected epithelial ovarian cancer, later confirmed to be other diagnosis than epithelial ovarian cancer or "cancer abdominis".
- • MRI incompatible devices or patient unable to undergo MRI.
About Region Västerbotten
Region Västerbotten is a leading healthcare authority in northern Sweden, dedicated to advancing medical research and improving patient care through innovative clinical trials. As a sponsor, Region Västerbotten focuses on collaborating with academic institutions, industry partners, and healthcare professionals to facilitate groundbreaking studies that address critical health challenges. With a commitment to ethical standards and patient safety, the organization aims to contribute to the global body of medical knowledge while enhancing the quality of healthcare services in the region. Through its robust infrastructure and expertise, Region Västerbotten strives to drive scientific discovery and foster an environment of excellence in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Umea, , Sweden
Patients applied
Trial Officials
Sara Strandberg, MD, PhD
Principal Investigator
Department of Radiation Sciences, Umea University/Radiology, Umea University Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported