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Retrospective Study of Reoperation After Primary Augmentation With NATRELLE® INSPIRA® Breast Implants

NCT02438332 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 330

Last updated 2016-07-25

No results posted yet for this study

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

  • Breast Implantation

Interventions

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

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Medical Director · Allergan

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02438332 on ClinicalTrials.gov