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ACTIVE NOT RECRUITING
NCT05316324
PHASE3

A Study of the Use of Acellular Dermal Matrix for Breast Reconstruction

Sponsor: Memorial Sloan Kettering Cancer Center

View on ClinicalTrials.gov

Summary

The researchers are doing this study to look at the number of complications that occur immediately after prepectoral breast reconstruction when Acellular Dermal Matrix (ADM) is used compared to when ADM is not used. These complications include infections, the need for Tissue Expander (TE) or implant removal, and other conditions that lead to additional surgery.

Official title: A Randomized Controlled Trial of Prepectoral Breast Reconstruction With and Without Acellular Dermal Matrix

Key Details

Gender

FEMALE

Age Range

21 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

353

Start Date

2022-03-23

Completion Date

2027-03

Last Updated

2026-02-17

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Prepectoral Breast Reconstruction with Acellular Dermal Matrix (ADM)

Prepectoral Breast Reconstruction with (ADM)

PROCEDURE

Prepectoral Breast Reconstruction without Acellular Dermal Matrix (ADM)

Prepectoral Breast Reconstruction without ADM

Locations (2)

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States

Memorial Sloan Kettering Nassau (Limited Protocol Activities)

Rockville Centre, New York, United States