Clinical Trials Directory

Trials / Completed

CompletedNCT06139588

Comparative Analysis of Two Animal-derived ADMs in Irradiated Implant-based Reconstruction

Comparative Study of the Efficacy and Risk Profile of Two Animal-derived Acellular Dermal Matrices in Patients Undergoing Mastectomy, Radiotherapy and Implant-based Reconstruction

Status
Completed
Phase
Study type
Observational
Enrollment
146 (actual)
Sponsor
European Institute of Oncology · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

The goal of this retrospective observational trial is to compare two different devices, used in implant-based breast reconstruction, called acellular dermal matrices, which are a sort of collagen patch that integrates with the tissues of the patient and helps in contrasting the collateral effects of radiotherapy (capsular contracture, implant loss) The main questions the study aims to answer are: * is one of the two matrices better than the other? (better results with fewer complications) * is there a group of patients who benefit more than another from the use of this type of devices? * is there an adm which works better in one specific subgroup of patients? Participants have undergone mastectomy, radiotherapy and implant reconstruction with the aid of two different kinds of acellular dermal matrices. Researchers will compare patients who receive the porcine-derived adm and the patients who receive bovine-derived adm to see if there is a difference in terms of capsular contracture reduction, aestethic result and complications.

Detailed description

Radiotherapy is highly effective in breast cancer treatment, yet it impairs satisfactory implant-based reconstruction, due to high rates of capsular contracture and implant loss. This said, a fervent investigtion exists upon solutions that can make implant-based reconstruction safer and aesthetically satisfying, including the use of acellular dermal matrices. We retrospectively want to analyze our ADM-assisted post-RT implant-based breast reconstructions comparing two different matrices (porcine and bovine), when autologous reconstruction was contraindicated, to assess eventual differences in efficacy and risk profile of the devices. We want to further stratify the population in 4 groups based on clinical presentation to assess if there was a group where ADMs proves to perform better (Group A - previous quadrantectomy, Group B - previous mastectomy and expander reconstruction, Group C - previous mastectomy and implant reconstruction, Group D - prior quadrantectomy followed by mastectomy and implant reconstruction).

Conditions

Interventions

TypeNameDescription
DEVICEacellular dermal matrix implant for breast reconstructionacellular dermal matrix implant in implant-based breast reconstruction in patients receiving radiotherapy

Timeline

Start date
2017-06-01
Primary completion
2022-12-31
Completion
2023-10-13
First posted
2023-11-18
Last updated
2023-12-13

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06139588. Inclusion in this directory is not an endorsement.