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Ovarian CancerNCT04724031

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

An observational study of Ovarian Cancer, run by Hellenic Cooperative Oncology Group at 1 site in Greece.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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

Who is it for?
Ages 18 to 80 years, women only
Conditions the study is for
Ovarian Cancer
What is being tested?
PARP inhibitor
How many people
180 participants
Where
1 siteGreece
Study dates
1 Nov 2019to 30 Apr 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • Women only
  • Adult, Older adult

Study population: women with advanced high grade ovarian cancer who receive Parp inhibitors at any line of treatmen

Who may be able to join

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

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Greece1 site
  • Adamantia Nikolaidi

    Athens, Attica, 15321

Other trials in Greece

About this study

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

Read the detailed description

A prospective-retrospective analysis of patients with histologically confirmed high grade ovarian cancer who will receive or received olaparib or niraparib will be conducted at any line of treatment.

Conditions
Ovarian Cancer
Being tested
PARP inhibitor
Medical subject headings
Ovarian Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PARP inhibitorDrug

    use at any line of treatment in patients with advanced ovarian cancer

Study groups in NCT04724031
Study groupRoleWhat they receive
One cohortwomen with advanced epithelial ovarian cancer who received PARP inhibitors at any line of treatment
Receives: Drug: PARP inhibitor

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Evaluation of Progression Free Survival

    Measured: 12/2022

Secondary outcomes (2)
  1. Assessment of the safety profile of olaparib in women with advanced high grade ovarian cancer

    Measured: 12/2021

  2. Assessment of the safety profile of niraparib in women with advanced high grade ovarian cancer

    Measured: 12/2021

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jan 2021
  2. Study start1 Nov 2019
  3. Primary completion9 Mar 2023
  4. Study completion30 Apr 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
180 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04724031
Sponsor's protocol ID
P420_PARP
Status last verified
Oct 2026
First submitted
17 Dec 2020
Last updated
19 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Ovarian Cancer, run by Hellenic Cooperative Oncology Group at 1 site in Greece.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Greece. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Evaluation of Progression Free Survival (time frame: 12/2022). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Oct 2026.

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