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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04031612
Other study ID # AB2009SEIN
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 9, 2009
Est. completion date September 2024

Study information

Verified date July 2019
Source Centre Georges Francois Leclerc
Contact AURELIE BERTAUT, MD, PHD
Phone +33 3 80 73 77 84
Email ABertaut@cgfl.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The NEOADJ Database base contains data collected during the regular clinical patient management (sociodemographic, clinical, pathological, radiological, biological, disease evolution...). This database allows easy access to information in a centralized and structured way.

This cohort is used to gather insights for research purposes. All data collected come from medical files of patients managed at Centre Georges Francois Leclerc, Dijon, France.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women followed for breast cancer in Georges Francois Leclerc Center

- Neoadjuvant chemotherapy

- Age >= 18

Exclusion Criteria:

- Males

- Metastatic breast cancer

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Neoadjuvant therapy
Neoadjuvant therapy

Locations

Country Name City State
France Methodology, Biostatistics and Data Management Unit Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Georges Francois Leclerc

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient survival Overall survival and evolution over years 5 years
Secondary Collection of patient and treatment characteristics Collection of patient and treatment characteristics over years, to set up prospective and retrospective studies 5 years