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European New Texture Implant Clinical Experience With Round Breast Implants

Breast Augmentation

Enrolled (actual)
18
Serious AEs
11.1%
Results posted
Jul 2015
Primary outcome: Primary: Investigator Overall Satisfaction With the Device Using a 5-Point Scale — 4.6 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
New texture round breast implants (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Allergan
Primary completion
Jan 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Investigator Overall Satisfaction With the Device Using a 5-Point Scale
4.6
SECONDARY
Subject Satisfaction With Breasts Using the BREAST-Q Questionnaire
89.3
SECONDARY
Investigator Evaluation of Whether the Implant is Palpably Distinguishable From the Tissue
2.7
SECONDARY
Percentage of Participants With Capsular Contracture Evaluated by Four-Grade Baker Scale
88.9; 11.1; 0.0; 0.0
SECONDARY
Percentage of Participants With Local Complications
16.7; 100.0; 11.1; 11.1; 5.6

Summary

The purpose of this study is to obtain clinical experience with the use of new texture, round breast implants in bilateral primary breast augmentation.

Eligibility Criteria

Inclusion Criteria

  • Be willing to undergo bilateral breast augmentation with subglandular, submuscular, or biplanar placement of the breast implants by inframammary approach only
  • Be a candidate for the device styles and sizes available in the study

Exclusion Criteria

  • Have tuberous breasts, congenital anomalies of the breast (e.g., Poland's Syndrome), or grade 3 ptosis
  • Have undergone any previous breast surgery
  • Have tissue covering determined inadequate or unsuitable by the surgeon
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01639742). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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