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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02878122
Other study ID # 35RC15_3007_FaCliBioCCo
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2015
Est. completion date March 2020

Study information

Verified date August 2021
Source Rennes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date March 2020
Est. primary completion date March 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Procedure:
Cancer treatment
Chemotherapy and laparoscopic surgery

Locations

Country Name City State
France LAVOUE Rennes

Sponsors (1)

Lead Sponsor Collaborator
Rennes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Chemoresistance defined by clinical recurrence 6 months after the end of chemotherapy
Primary Chemoresistance defined by biological recurrence 6 months after the end of chemotherapy
Primary Chemoresistance defined by radiological recurrence 6 months after the end of chemotherapy
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