Study of Sentinel Lymph Node Assessment Following Previous Surgical Biopsy for Early Breast Cancer

NCT00293865 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 203

Last updated 2016-04-19

No results posted yet for this study

Summary

The purpose of this study is to assess the detection rate and false negative rate of sentinel lymph node biopsy following previous surgical biopsy for early breast cancer diagnosis.

Conditions

Interventions

PROCEDURE

sentinel node

detection of the sentinel node in breast cancer

PROCEDURE

GAS

Sponsors & Collaborators

  • Institut Cancerologie de l'Ouest

    lead OTHER

Principal Investigators

  • Jean Marc Classe, MD · Centre Rene Gauducheau

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2012-03-31
Completion
2012-03-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00293865 on ClinicalTrials.gov