IDENTIFICATION OF SENTINEL NODE(S) IN BREAST CANCER

NCT01790399 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 115

Last updated 2014-03-06

No results posted yet for this study

Summary

The study is based on the identification of sentinel node(s) by SENTIMAG / SIENNA + in addition to the usual method (blue and /or radioactive product). This is a feasibility study

Conditions

Interventions

PROCEDURE

Excision of sentinel node(s)

Excision of sentinel node(s) using SENTIMAG / SIENNA + in addition to the usual method (blue and /or radioactive product)

Sponsors & Collaborators

  • Sysmex America, Inc.

    collaborator INDUSTRY
  • Centre Oscar Lambret

    lead OTHER

Principal Investigators

  • Jean-Louis MD HOUPEAU · Centre Oscar Lambret

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2014-02-28
Completion
2014-07-31

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 NCT01790399 on ClinicalTrials.gov