Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Axillary Adenopathy
  • Breast Cancer
  • Radiotherapy Side Effect
  • Therapy-Associated Cancer
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: A prospective, randomized, multicenter study.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

A prospective, randomized, open-label, parallel-assigned, multicenter, phase III study. The estimated sample size is 1.666 patients, over 5 years. Patients will be stratified and analyzed independently according to the neoadjuvant treatment regimen, whether chemotherapy (CT) +/- hormonal therapy (HT...

A prospective, randomized, open-label, parallel-assigned, multicenter, phase III study. The estimated sample size is 1.666 patients, over 5 years. Patients will be stratified and analyzed independently according to the neoadjuvant treatment regimen, whether chemotherapy (CT) +/- hormonal therapy (HT).

Tracking Information

NCT #
NCT04889924
Collaborators
Not Provided
Investigators
Principal Investigator: Maria Laplana, MD Institut Catala de Oncologia Principal Investigator: Amparo Garcia-Tejedor, MDPhD Hospital Universitari de Bellvitge