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OpenTrials
Completed

NCT Number: NCT02878122

Study of Predictive Factors of Chemoresistance in Ovarian Cancer

Epithelial ovarian cancer (EOC) has a poor prognosis. EOC management requires debulking surgery and chemotherapy based on taxol and carboplatine. Initial response is often good, but most often a recurrence occurred in the first 18 months. Early recurrence signs chemoresistance and palliative treatment. The study of predictive clinical or biological factors is required to adapt therapeutic and develop new treatments.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patient > 18 years of age
  • patient with histological proven epithelial ovarian cancer

Exclusion criteria

  • patients who can not give their own consent
  • patients without ovarian cancer

Treatment and study plan

Cancer treatment

Procedure

Chemotherapy and laparoscopic surgery

Other names: Carboplatin, Taxol

Primary outcomes

  1. Chemoresistance defined by clinical recurrence

    Time frame: 6 months after the end of chemotherapy

  2. Chemoresistance defined by biological recurrence

    Time frame: 6 months after the end of chemotherapy

  3. Chemoresistance defined by radiological recurrence

    Time frame: 6 months after the end of chemotherapy

Sponsors and collaborators

Lead sponsor

Rennes University Hospital

Other

Registry information

Acronym: FaCliBioCCo

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Aug 25, 2016
Registry last updated
Aug 17, 2021

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.

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