Trials / Completed
CompletedNCT02438332
Retrospective Study of Reoperation After Primary Augmentation With NATRELLE® INSPIRA® Breast Implants
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 330 (actual)
- Sponsor
- Allergan · Industry
- Sex
- Female
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the incidence of reoperations associated with the use of smooth and textured NATRELLE® INSPIRA® TruForm® 1 and TruForm® 2 devices in patients who have undergone primary breast augmentation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Smooth NATRELLE® INSPIRA® TruForrm® 1 Breast Implants | Surgical implant |
| DEVICE | Textured NATRELLE® INSPIRA® TruForm® 1 Breast Implants | surgical implant |
| DEVICE | Smooth NATRELLE® INSPIRA® TruForrm® 2 Breast Implants | surgical implant |
| DEVICE | Textured NATRELLE® INSPIRA® TruForm® 1 Breast Implants | surgical implant |
Timeline
- Start date
- 2014-12-01
- Primary completion
- 2016-06-01
- Completion
- 2016-06-01
- First posted
- 2015-05-08
- Last updated
- 2016-07-25
Locations
17 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT02438332. Inclusion in this directory is not an endorsement.