Clinical Trials Directory

Trials / Completed

CompletedNCT00052676

Technetium Tc 99m Sulfur Colloid and Blue Dye In Detecting Sentinel Lymph Nodes in Patients With Breast Cancer

French Randomized Sentinel Node Multicentric Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Centre Paul Strauss · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: It is not yet known whether injecting technetium Tc 99m sulfur colloid and blue dye near the tumor is more effective than injecting them near the nipple in identifying sentinel lymph nodes in patients with stage I or stage II breast cancer. PURPOSE: Randomized diagnostic trial to compare the effectiveness of injecting technetium Tc 99m sulfur colloid and blue dye near the tumor with that of injections around the nipple in detecting sentinel lymph nodes in patients who have stage I or stage II breast cancer.

Detailed description

OBJECTIVES: * Determine the optimal mode of injection (peritumoral vs periareolar) of patent blue V dye and technetium Tc 99m sulfur colloid in patients with stage I or II breast cancer undergoing sentinel lymph node identification. * Determine the reduction of morbidity associated with breast cancer surgery, in terms of local control and survival, in patients undergoing sentinel lymph node identification with these drugs. * Determine the evolution of disease in patients who have undergone this procedure and do not show histological invasion of the sentinel lymph node. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive peritumoral injections of patent blue V dye and technetium Tc 99m sulfur colloid. * Arm II: Patients receive periareolar injections as in arm I. Patients in both arms showing histological metastasis of the sentinel lymph node or without identification of the sentinel lymph node undergo standard axillary lymph node dissection. Patients are followed for disease evolution. PROJECTED ACCRUAL: A total of 450 patients (225 per arm) will be accrued for this study within 2-2.5 years.

Conditions

Interventions

TypeNameDescription
DRUGpatent blue V dye
PROCEDUREradionuclide imaging
PROCEDUREsentinel lymph node biopsy
RADIATIONtechnetium Tc 99m sulfur colloid

Timeline

Start date
2002-10-01
Completion
2007-05-01
First posted
2003-01-27
Last updated
2013-05-15

Locations

7 sites across 1 country: France

Source: ClinicalTrials.gov record NCT00052676. Inclusion in this directory is not an endorsement.