Observational, Bi-directional (Prospective and Retrospective) Study for Patients With Newly Diagnosed Ovarian Cancer Stages IA to IVB, or Persistent or Recurrent Disease From January 2021; Irrespective of Histology

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorAstraZeneca

About this trial

The findings from this study have the potential to serve as a foundation for evaluating the current practices related to surgical procedures, systemic therapies, hyperthermic intraperitoneal chemotherapy, and referrals to geneticists for OC patients. By identifying the strengths and weaknesses of the existing care, this project intends to generate valuable insights that can lead to the implementation of quality parameters for the treatment of ovarian cancer in the country.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients ≥18 years old;

Newly diagnosed ovarian cancer stages IA to IVB, or persistent or recurrent disease from January 2021;

Irrespective of histology

Disqualifiers

Borderline tumors;

Pregnancy;

Synchronous tumor or second primary in the last 5 years (except thyroid cancer and non-melanoma skin cancer);

Trial population

The study base consists of patients newly diagnosed with ovarian cancer across stages IA to IVB, and those with persistent or recurrent disease, diagnosed from January 2021 onwards.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

250 Participants
are grouped into 1 trial group
Group A: Group 1

Trial outcomes

Primary outcomes

1

Description of socio-demographic characteristics

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are begin performed for the primary outcomes of this study.

Time frame
Throught study a completation, an average of 3 years
2

Description of pathological characteristics

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are being performed for the primary outcomes of this study.

Time frame
Throught study a completation, an average of 3 years
3

Description of treatment

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are being performed for the primary outcomes of this study.

Time frame
Throught study a completation, an average of 3 years

Secondary outcomes

1

Treatment interval of systemic therapy in metastatic disease

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are beign performed for the outcomes of this study.

Time frame
Throught study a completation, an average of 3 years
2

Disease free-survival

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are beign performed for the outcomes of this study.

Time frame
Throught study a completation, an average of 3 years
3

Time to next chemotherapy

The study's findings could provide a basis for evaluating current practices in ovarian treatment and other characteristics about this disease. By identifying strengths and weaknesses in existing care, the project aims to offer insights that may lead to the implementation of quality parameters for ovarian cancer treatment in the country. No formal statistical comparisons are beign performed for the outcomes of this study.

Time frame
Throught study a completation, an average of 3 years

Other outcomes

Sponsors and contacts

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