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Clinical Trial Summary

The objective of this interventional study is based on the hypothesis that coelioscopique surgery could be used to reduce breast hypertrophy. This study can be expected to scientifically validate the use of laparoscopic surgery to obtain a clinical result in the context of reduction of medium volume breast hypertrophy.


Clinical Trial Description

Breast reductions are common procedures. One of the main difficulties related to this surgery remains the healing, wide at the peri-areolar level, vertical at the sub-areolar level and in the sub-mammary fold. In addition, this intervention remains subject to the vagaries of hypertrophic or even keloidal healing, especially in young subjects. On This study can be expected to scientifically validate the use of laparoscopic surgery to obtain a clinical result without scarring in the context of the reduction of medium volume breast hypertrophy. Ultimately, the results of this study may serve as a basis for further research by proposing: - Prophylactic mastectomies and immediate breast reconstruction without lateral scar and with a less visible sub-breast scar. - A breast reduction in young patients before the skin undergoes the effects of the heaviness of the breasts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05822115
Study type Interventional
Source Groupe Hospitalier Nord-Essonne
Contact Eric Dr DUNET, Chirurgien
Phone +33607812501
Email ericdunet@gmail.com
Status Recruiting
Phase N/A
Start date April 24, 2023
Completion date September 2024

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Recruiting NCT05891613 - A Study of Liposomal Bupivacaine Versus 0.25% Bupivacaine Hydrochloride Post Breast Reduction Phase 4