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Personalised Program for Women Treated for Hodgkin Disease (PROPER)

I

Institut Paoli-Calmettes

Status

Terminated

Conditions

Breast Cancer
Hodgkin Disease

Treatments

Procedure: intensive screening

Study type

Interventional

Funder types

Other

Identifiers

NCT01188915
PROPER/IPC 2010-001

Details and patient eligibility

About

After treatment for Hodgkin disease, secondary cancer, in particular breast cancer induced by treatment, are the first cause of death.

The investigators will estimate the risk to develop breast cancer in this population of women treated for hodgkin disease, and will propose women at high rish to participate in an intensive screening program based on an annual detection based on mammography, echography, and RMI.

Enrollment

51 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • women > 18 years
  • treated for Hodgkin disease
  • signed informed consent
  • high risk of breast cancer

Exclusion criteria

  • patients unable to have a regular follow-up

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

51 participants in 1 patient group

intensive screening
Experimental group
Description:
annual breast cancer detection based on mammography, echography and RMI.
Treatment:
Procedure: intensive screening

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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