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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03831230
Other study ID # 2018-A02152-53
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 7, 2019
Est. completion date August 2029

Study information

Verified date July 2021
Source Centre Francois Baclesse
Contact Enora DOLIVET, MD
Phone 02 31 45 50 50
Email e.dolivet@baclesse.unicancer.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Development of ex vivo models of ovarian cancer, fallopian tubes or peritoneum.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date August 2029
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient over 18 years old. - Patient with ovarian cancer, carcinoma of the fallopian tubes, or histologically proven peritoneum. All FIGO stages are accepted for the study. - Patient to be managed by surgery (laparoscopy and / or laparotomy). Exclusion Criteria: - Pregnant woman - Persons deprived of liberty or guardianship (including curatorship) - History of any other clinically active malignancy in the last 5 years prior to inclusion

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
collection of blood, urine, tumor and ascite samples
collection of blood, urine, tumor and ascite samples during ovarian surgery

Locations

Country Name City State
France Centre François BACLESSE Caen

Sponsors (1)

Lead Sponsor Collaborator
Centre Francois Baclesse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rates of exploitable ex vivo tumor, blood and urine samples for performing predictive tests Number and quality of tumor, blood and urine samples that can be used to perform predictive tests of the response to treatment Collection of blood, urine, tumor and ascite samples at the time of ovarian surgery
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