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Evaluation of the Effectiveness of Prepectoral Breast Reconstruction

NCT05125991 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2023-08-24

No results posted yet for this study

Summary

The study plans to compare conventional submuscular reconstruction with definitive implant and muscle sparing reconstruction with definitive implant in selected patients. The two techniques are compared in terms of patient quality of life and satisfaction; patient related outcomes, reconstruction morbidity, early and late complications are also investigated.

Conditions

Interventions

PROCEDURE

Prepectoral reconstruction

Prepectoral breast reconstruction

PROCEDURE

Submuscolar reconstruction

Submuscolar breast reconstruction

Sponsors & Collaborators

  • European Institute of Oncology

    lead OTHER

Principal Investigators

  • Francesca De Lorenzi, PhD, MD · European Institute of Oncology

  • Paolo Veronesi, MD · European Institute of Oncology

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-03
Primary Completion
2024-06-30
Completion
2024-12-31

Countries

  • Italy

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05125991 on ClinicalTrials.gov