Primary Aesthetic Breast Augmentation: Comparative Study Between Breast Implants and Autograft of Adipose Tissue

Recruiting

• Conditions: Breast Implants

• Registration Number: NCT06147661
• Lead Sponsor: University Hospital, Strasbourg, France

Brief Summary

The use of autograft of adipose tissue for aesthetic breast augmentation is increasing year after year. According to the latest meta-analysis of 2016, autograft of adipose tissue in augmentation mastoplasty seems to be a promising method with a satisfactory resorption volume and patient and surgeon satisfaction. However, this technique allows for small to moderate breast augmentation and is therefore not suitable for patients wanting a significant increase.

Breast prostheses allow a significant increase. Numerous studies have shown an improvement in patient satisfaction and quality of life assessed using the BREAST-Q questionnaire.

On the other hand, very few studies have objectively evaluated the satisfaction of patients who have benefited from an autograft of adipose tissue as part of aesthetic breast augmentation. No study has yet compared the satisfaction of patients who have benefited from breast implants or lipofilling.

The aim of this study is to compare the satisfaction of patients who have benefited from breast augmentation by prosthesis or by lipofilling using a remote satisfaction interview.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-01
• Status Verified: 2023-10
• Study First Submitted: 2023-10-26
• Study First Submitted QC: 2023-11-22
• Last Update Submitted: 2023-11-22
• Study First Posted: 2023-11-27
• Last Update Posted: 2023-11-27
• Primary Completion: 2024-01
• Study Completion: 2024-01-22

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 119

Inclusion Criteria

• Adult woman (age ≥ 18 years)
• having benefited from primary aesthetic breast augmentation at Strasbourg University Hospital between June 27, 2017 and June 27, 2022
• not opposing the reuse of its data for scientific research purposes.

Exclusion Criteria

• Woman who expressed her opposition to the reuse of her data for scientific research purposes
• Woman with a breast malformation: tuberous breasts or breast asymmetry of more than one cup
• Woman with comprehension difficulties
• Woman under guardianship or curatorship

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient woman satisfaction	1 to 4 years after breast implants	This satisfaction will be assessed using a remote satisfaction interview

Trial Locations

Locations (1)

Service de Chirurgie Plastique, Reconstructrice et Esthétique - CHU de Strasbourg - France; 🇫🇷 Strasbourg, France