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

NCT ID: NCT04724031

Last Updated: 2023-03-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-11-01

Study Completion Date

2023-09-30

Brief Summary

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

Detailed Description

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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

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Ovarian Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Study Groups

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One cohort

women with advanced epithelial ovarian cancer who received PARP inhibitors at any line of treatment

PARP inhibitor

Intervention Type DRUG

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

Interventions

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PARP inhibitor

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

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hellenic Cooperative Oncology Group

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Adamantia Nikolaidi

Athens, Attica, Greece

Site Status

Countries

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Greece

Other Identifiers

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P420_PARP

Identifier Type: -

Identifier Source: org_study_id

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