Clinical Trials Directory

Trials / Completed

CompletedNCT03556397

Sentinel Lymph Node Biopsy in Patients With Breast Cancer After Neoadjuvant Therapy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
61 (actual)
Sponsor
University Hospital Ostrava · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to create clear indications for Sentinel Lymph Node Biopsy (SLNB) or Axillary Dissection (AD) in women with breast carcinoma after neoadjuvant therapy by studying the false negative rate of SLNB.

Detailed description

The main object of the study is to evaluate, whether sentinel lymph node biopsy (SLNB) at women with breast cancer after neoadjuvant therapy is a method with a high false-negative rate. Patients will be classified into groups according to histological findings during SLNB, clinical and ultrasonography (USG) findings in the axilla. The aim of this study is to create clear indications for SLNB or axillary dissection (AD). In case of extension of SLNB indications, there will be a decrease in morbidity after surgical therapy when compared to AD, which will mean a profit for the patients.

Conditions

Interventions

TypeNameDescription
PROCEDURESentinel lymph node biopsy (SLNB)Sentinel lymph node biopsy will be performed in the patients
PROCEDUREAxillary dissectionAxillary dissection procedure will be performed in the patients

Timeline

Start date
2018-01-01
Primary completion
2020-11-30
Completion
2020-11-30
First posted
2018-06-14
Last updated
2021-02-18

Locations

2 sites across 1 country: Czechia

Source: ClinicalTrials.gov record NCT03556397. Inclusion in this directory is not an endorsement.