Status:

COMPLETED

Research for Predictive Biologic Parameters of Cutaneous Hypersensitivity After Brachytherapy in Breast Cancer

Lead Sponsor:

Centre Oscar Lambret

Conditions:

Breast Cancer

Eligibility:

FEMALE

60+ years

Phase:

NA

Brief Summary

25 patients, treated by brachytherapy in a phase II study "Mammosite" (from 2003 to 2005), will be asked to attend a clinical exam in order to evaluate the late cutaneous toxicity due to brachytherapy...

Detailed Description

This is an interventional study for the french law

Eligibility Criteria

Inclusion

  • All patient treated by exclusive per-operative brachytherapy in the prior study Mammosite for breast cancer
  • Patient with social security

Exclusion

  • Not applicable

Key Trial Info

Start Date :

September 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2009

Estimated Enrollment :

25 Patients enrolled

Trial Details

Trial ID

NCT00922961

Start Date

September 1 2008

End Date

February 1 2009

Last Update

July 23 2012

Active Locations (1)

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Centre Oscar Lambret

Lille, France, 59020