Registry Trial to Evaluate the Clinical Utilization of Targeted Axillary Dissection (TAD)

CompletedOBSERVATIONAL
Enrollment

548

Participants

Timeline

Start Date

February 1, 2017

Primary Completion Date

February 28, 2019

Study Completion Date

October 1, 2019

Conditions
Early Stage Breast Cancer
Interventions
OTHER

Not suitable for TAD

Registry of the rate of patients not suitable for TAD as initial CNB with clip placement of axillary lymph nodes is not possible and underlying medical contraindications, technical obstacles or miscellaneous reasons why needle biopsy and/or clip labeling of clinically affected lymph nodes cannot be done

PROCEDURE

Suitable for TAD

Registry of surgical outcome measures of targeted resection of the clipped node with optional sentinel node biopsy or axillary lymph node dissection with or without preceding neoadjuvant chemotherapy

Trial Locations (3)

45136

Kliniken Essen-Mitte, Essen

45879

Evangelische Kliniken Gelsenkirchen, Gelsenkirchen

73730

Klinikum Esslingen, Esslingen am Neckar

All Listed Sponsors
collaborator

GBG Forschungs GmbH

OTHER

lead

Kliniken Essen-Mitte

OTHER

NCT03102307 - Registry Trial to Evaluate the Clinical Utilization of Targeted Axillary Dissection (TAD) | Biotech Hunter | Biotech Hunter