RecruitingNCT03862677
Determining Prognostic Immune Markers in Patients With Ovarian Cancer
Sponsor
Leiden University Medical Center
Enrollment
300 participants
Start Date
Aug 15, 2020
Study Type
OBSERVATIONAL
Conditions
Summary
The IMPRoVE study is a prospective, non-interventional, explorative cohort study to determine prognostic immune markers in patients with epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer (EOC).
Eligibility
Sex: FEMALEMin Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is collecting blood and tumor tissue samples from women with ovarian cancer — at the time of surgery and during follow-up — to identify immune markers in the tumor environment that may help predict how well patients respond to treatment and how their disease will progress.
**You may be eligible if...**
- You are 18 years or older
- You have been diagnosed with (or are suspected to have) primary or recurrent epithelial ovarian cancer (EOC) and are scheduled for surgery, chemotherapy, or immunotherapy
- You are in good general health (WHO performance status 0–2)
- You are accessible for ongoing treatment and follow-up visits
- You have given written informed consent
**You may NOT be eligible if...**
- You have had another active cancer in the past 5 years (except treated non-melanoma skin cancer)
- You have a known serious infection such as HIV, or hepatitis A, B, or C
- You are receiving immune-suppressing medications
- You have a medical or psychological condition that would prevent you from completing the study
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
OTHERNo intervention
Observational study, no intervention
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03862677
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