Understanding Patient Preferences for PARP Inhibitors in Ovarian Cancer

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on patients with ovarian cancer who have defective DNA repair mechanisms and examines their preferences for maintenance therapy using PARP inhibitors (PARPi). It involves performing HRD testing to personalize treatment options based on the patients' responses to platinum-based chemotherapy. The study aims to evaluate treatment outcomes and quality of life in a real-world setting, providing insights into the efficacy and cost-effectiveness of PARPi therapy, particularly niraparib. By utilizing decision aids, the study seeks to empower patients in their treatment choices.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Known or suspected stage 3/4 high grade serous or endometrioid ovarian cancer Able to provide oral consent and complete questionnaires in English as per study protocol

Exclusion Criteria:

* Ineligible for Maintenace PARPi therapy Refusal to undergo HRD testing

Where it's running

• Saskatchewan Cancer Center
  Saskatoon, S, Canada Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.