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NCT Number: NCT06535334

Intraperitoneal Chemotherapy in Recurrent Ovarian Cancer

This study aims to compare intravenous chemotherapy versus intraperitoneal chemotherapy in patients with recurrent ovarian cancer.

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Key information

Age range

20 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Department of Obstetrics and Gynecology, Far Eastern Memorial Hospital

Banqiao District, New Taipei, 22050, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • women who had recurrent ovarian cancer and was treated with either intravenous or intraperitoneal platinum based chemotherapy

Exclusion criteria

  • women who did not complete the designated treatment course (exception to those who had to quit due to progressive disease or death of any cause)

Treatment and study plan

Chemotherapy

Drug

Intravenous chemotherapy versus intraperitoneal chemotherapy in recurrent ovarian cancer

Primary outcomes

  1. RFS

    Time frame: the time interval from the date of surgery or the start of chemotherapy to clinically defined recurrence, disease progression, death from any cause or last follow-up

    Recurrence free survival

  2. OS

    Time frame: the time interval from the date of surgery or the start of chemotherapy to the date of death from any cause or last follow-up

    Overall Survival

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Official study title

Intravenous Chemotherapy Versus Intraperitoneal Chemotherapy in Recurrent Ovarian Cancer

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Aug 2, 2024
Registry last updated
Aug 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.