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Clinical Trials/NCT01114464
NCT01114464
Terminated
Not Applicable

Impact of Chemotherapy on Ovarian Reserve in Young Women With Breast Cancer

Nantes University Hospital11 sites in 1 country250 target enrollmentJanuary 2010
ConditionsOvarian Reserve

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ovarian Reserve
Sponsor
Nantes University Hospital
Enrollment
250
Locations
11
Primary Endpoint
To evaluate the effects of adjuvant or neoadjuvant chemotherapy treatment on ovarian reserve for in situ breast cancer patients
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

The aim of this protocol is to study the deleterious impact of adjuvant chemotherapy or neoadjuvant chemotherapy on ovarian reserve in young women suffering from breast cancer. A new relevant ovarian reserve marker, serum Anti-Mullerian Hormone, will be used in order to evaluate precisely the impact of chemotherapy on ovaries during chemotherapy administrations and after during follow-up (24 months). This strategy offers 2 main advantages : no modification of the traditional care of patients (treatment, organisation, follow up ...) and use of a non invasive marker (serum). The final objective is to give precise information to patients on their future fertility after remission.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
April 2014
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • female 18-39 years
  • suffering from breast cancer
  • treated with adjuvant or neoadjuvant chemotherapy

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

To evaluate the effects of adjuvant or neoadjuvant chemotherapy treatment on ovarian reserve for in situ breast cancer patients

Time Frame: 24 months

Serum anti-Müllerian hormone concentration will be measured at each chemotherapy administration and 24 months follow-up after chemotherapy completion

Study Sites (11)

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