Status:
RECRUITING
An Analysis of Adverse Events and Satisfaction Outcomes of Women Who Underwent Primary and Secondary Breast Augmentation Using Silimed® Breast Implants
Lead Sponsor:
Silimed Industria de Implantes Ltda
Conditions:
Breast Implant; Complications
Quality of Life
Eligibility:
FEMALE
18+ years
Brief Summary
The study investigates the safety and performance of Silimed® silicone gel breast implants with a textured surface and Silimed® silicone gel breast implants with polyurethane coated surface. Female pa...
Eligibility Criteria
Inclusion
- provide written informed consent.
- female at birth
- be 18 years of age or older
- have received breast implant(s) for indication of primary or secondary augmentation until 21 days before (including the visit window)
- having received a breast implant with a textured surface or a breast implant with a surface coated with Silimed® polyurethane foam
- ability to comply with the protocol throughout the follow-up period.
Exclusion
- mammary reconstruction in at least one breast or augmentation after previous reconstruction,
- pregnancy informed or breastfeeding at the inclusion moment,
- advanced fibrocystic disease at the time of implantation,
- neoplasia of any type not yet treated or being treated at the time of implantation, infection in activity not yet treated or being treated at any site at the time of implantation,
- reporting or recording of adverse reactions or intolerance to polyurethane or silicone prior to implantation,
- immune diseases affecting active connective tissue or (eg, lupus erythematosus, discoid lupus, scleroderma, etc.) at the time of implantation,
- signs of inflammation of the breast or implant site at the time of implantation,
- Increased risk of immediate postoperative complications due to use of illicit drugs or medications,
- Increased risk of immediate post-surgical complications caused by illicit drug use or medication use,
- have participated in another clinical study up to 6 months prior to the placement of the implant,
- any other condition which, based on the opinion of the investigator or designee, may prevent the provision of informed consent, renders participation in the study is unsafe, compromises adherence to the protocol, complicates the interpretation of data from the study outcome, or otherwise interferes with the achievement of study objectives.
Key Trial Info
Start Date :
July 31 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2035
Estimated Enrollment :
632 Patients enrolled
Trial Details
Trial ID
NCT03356132
Start Date
July 31 2018
End Date
December 1 2035
Last Update
December 3 2024
Active Locations (1)
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1
Perfektua Serviços Médicos Ltda
Niterói, Rio de Janeiro, Brazil, 24230-052