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NCT04724031Completed

Real World Data Analysis of PARP Inhibitors Use in Patients With Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 19 Oct 2026

Brief summary (registry, in English)

Real-world clinical outcomes and toxicity data will be evaluated in patients with advanced high grade ovarian cancer who will receive PARP inhibitors.

Status (registry)
Completed
Study type
Observational
Enrollment
180 (actual)
First submitted
17 Dec 2020
Start date
1 Nov 2019
Primary completion date
9 Mar 2023
Lead sponsor
Hellenic Cooperative Oncology Group
NCT number
NCT04724031

What you commit to

  • Study type: Observational
  • Participants enrolled: 180
  • From 1 Nov 2019 to the primary completion date, 9 Mar 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \-

Who the study is looking for

  • \- women \>18 years old with advanced high grade ovarian cancer

Age in the registry: 18 years to 80 years · Sex: Female

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Adamantia Nikolaidi
Coordinator of this site? Confirm its status
AthensGreeceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.