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Clinical Trial Summary

The purpose of the study is to collect data regarding the aesthetic outcomes of patients who had breast reduction surgery and /or mastopexy in terms such as scaring, patient satisfaction, breast ptosis assessment including taking photographs and filling questionnaires.


Clinical Trial Description

This is a prospective observational study, single center cohort to explore the aesthetic outcomes of patients who had breast reduction and / or mastopxy surgery. The surgical intervention will be determined by the clinician with no correlation to this study.

The study will focus on the aesthetic aspects of the clinical outcome resultant from the breast surgery in par course of 5 years. Scar tissue assessment and patient's reported data (satisfaction and well-being) will be collected.

Suitable patients will be assessed for study eligibility at a screening visit and, if eligible, will be scheduled for breast surgery according to the patient and surgeon discretion.

At each follow up visit, patients will undergo clinical general examination, breast and ptosis endearments, scar appearance , aesthetic evaluation. Patients will fill satisfaction questionnaires ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02016677
Study type Observational
Source Orbix Medical Ltd.
Contact
Status Terminated
Phase N/A
Start date December 2013
Completion date November 2015

See also
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Completed NCT00986453 - PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction N/A
Completed NCT02769559 - Reduction Mammaplasty and Improved Quality of Life N/A
Completed NCT00558246 - Study of Prineo (Dermabond Protape) Versus Sutures in Breast Procedures Phase 4
Recruiting NCT05898087 - Subpectoral Bupivacaine for Pain Management in Adolescent Reduction Mammaplasty Phase 4