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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04130373
Other study ID # 1955K
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date June 1, 2019
Est. completion date June 2020

Study information

Verified date October 2019
Source Humanitas Clinical and Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Autologous fat grafting, also known as lipofilling, is a surgical technique consisting in the processing and transfer of adipose tissue from one area in our organism (hips, thighs) to region which in need of reconstructive and aesthetic correction. The technique is frequently used after radical or conservative mammary surgery, aiming to achieve better aesthetic results, reduce pain induced by both surgery and radiotherapy. The scientific community was widely involved in the debate regarding the use of mesenchymal/stem cells in a patient with high risk of tumor progression due to their elevated proliferative profile. This study aims to retrospectively evaluate the oncological safety in the use of lipofilling in patients who underwent oncological and reconstructive treatment in our Institute.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 6510
Est. completion date June 2020
Est. primary completion date January 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- female

- breast carcinoma (any histological type, carcinoma in situ included) treated with radical or conservative surgery

- group treated with lipofilling and group which didnt receive lipofilling

- timing: retrospective evaluation of cases form 2006 to 2016, with a minimum of two year follow up

Exclusion Criteria:

- neoplasie different from infiltrating and in sutu breast carcinoma

- in situ lobular carcinoma

- patients with breast carcinoma and metastasis

- lipofilling procedure used before the oncological treatment for breast carcinoma

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Autologous fat grafting procedure
Surgical intervention based on the injection of autologous fat grafting after radical or conservative breast surgery and breast reconstruction.
Breast reconstruction
Breast reconstructive procedures after oncological radical or conservative breast surgery

Locations

Country Name City State
Italy Istituto Clinico Humanitas Rozzano Milan

Sponsors (1)

Lead Sponsor Collaborator
Humanitas Clinical and Research Center

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oncological safety of autologous fat grafting Percentage of disease relapse in loco Two years
Secondary Establishment of timing in disease relapse Two years
Secondary Establish the distribution in disease relapses Establish the distribution in disease relapse in thre different histological subtypes of breast carcinoma Two years
Secondary Establish overall survival rate in experimental and control groups Two years
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