MedPath

Sentinel Node And Recurrent Breast cancer

Recruiting
Conditions
Recurrent breast cancerSentinel node biopsieRecidief mammacarcinoomSchildwachtklierprocedure
Registration Number
NL-OMON22722
Lead Sponsor
The principal investigator of this study is mrs. A. Maaskant-Braat, resident surgery
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
150
Inclusion Criteria

1. Women above 18 years old with locally recurrent breast cancer after earlier BCT or modified radical mastectomy.

2. Operable cytological /histological confirmed locally recurrent breast cancer.

Exclusion Criteria

1. Proven ipsi- or contralateral regional lymph node metastases (ultrasound and FNA).

2. Known to be allergic to 99mTc-colloidal albumin” or blue dye injection fluids.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
- Registration of technical feasibility of lymphatic mapping and sentinel node biopsy in patients with locally recurrent breast cancer.<br /><br>- Registration of success rate of lymphatic mapping and SNB in patients with locally recurrent breast cancer.<br /><br>- Registration of validity of lymphatic mapping and sentinel node biopsy in patients with locally recurrent breast cancer. <br><br><br>
Secondary Outcome Measures
NameTimeMethod
- Registration of lymphatic drainage pathways in patients with locally recurrent breast cancer. <br /><br>- Registration of sentinel lymph node status in patients with locally recurrent breast cancer. <br /><br>- Registration of possible influence of lymphatic mapping and SNB on therapeutic decisions in patients with locally recurrent breast cancer. <br /><br><br>
© Copyright 2025. All Rights Reserved by MedPath