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Breast Cancer and Chemo-amennorhea (chemo-ameno)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01867229
Recruitment Status : Completed
First Posted : June 3, 2013
Last Update Posted : April 10, 2019
Sponsor:
Information provided by (Responsible Party):
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Brief Summary:
Relation between chemotherapy and amennorhea

Condition or disease Intervention/treatment
Breast Cancer Other: observational

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Study Type : Observational
Actual Enrollment : 7 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Etude Prospective Multicentrique de l'aménorrhée Chimio-induite et de sa réversibilité Dans le Cancer du Sein Chez Des Patientes préménopausées Recevant Une chimiothérapie Adjuvante ou néoadjuvante. Etude Améno-Chimio.
Study Start Date : October 2011
Actual Primary Completion Date : December 2013
Actual Study Completion Date : December 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Group/Cohort Intervention/treatment
FEC- TC
Fluorouracil- Epiadriamycine- Cyclophosphamide Taxotère-Cyclophosphamide
Other: observational
standard of care fore patients with non metastatic breast cancer




Primary Outcome Measures :
  1. incidence and duration of the amenorrhea induced by chemotherapy [ Time Frame: 5 years ]


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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
pre-menauposal breast cancer treated with chemotherapy
Criteria

Inclusion Criteria:

pre-menauposal breast cancer needed to be treat with chemotherapy -

Exclusion Criteria:

metastases menopausal

-


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01867229


Locations
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Belgium
Clinique Saint Vincent
Rocourt, Liège, Belgium, 4000
Cliniques Universitaires Saint-Luc
Brussels, Belgium, 1200
Centre Hospitalier Université de Liège
Liège, Belgium, 4000
CHR Citadelle
Liège, Belgium, 4000
Centre hospitalier Peltzer La Tourelle
Verviers, Belgium, 4800
France
Institut Claudius Renaud
Toulouse, France, 31059
Sponsors and Collaborators
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Investigators
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Principal Investigator: jean-Pascal Machiels UCL-Saint Luc

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Responsible Party: Cliniques universitaires Saint-Luc- Université Catholique de Louvain
ClinicalTrials.gov Identifier: NCT01867229     History of Changes
Other Study ID Numbers: UCL-gyneco-001
2009/07DEC/377 ( Other Identifier: CEHF )
First Posted: June 3, 2013    Key Record Dates
Last Update Posted: April 10, 2019
Last Verified: April 2019

Keywords provided by Cliniques universitaires Saint-Luc- Université Catholique de Louvain:
pre-menauposal
neo-adjuvant or adjuvant chemotherapy
no metastases

Additional relevant MeSH terms:
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Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases