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Observational Study to Assess Long-Term Follow-Up of Breast Augmentation Subjects

NCT01076686 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 94

Last updated 2012-05-14

Study results available
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Summary

A history and physical focused on clinical sequelae of breast implant rupture was completed by patients to assess long-term clinical sequelae of SKY0402 and its relation to the silicon shell.

Conditions

  • Postoperative Pain

Interventions

DRUG

Questionnaire and Physical Exam

A 10-question survey and a six-item physical exam were completed.

Sponsors & Collaborators

  • Pacira Pharmaceuticals, Inc

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2010-03-31
Completion
2010-03-31

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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 NCT01076686 on ClinicalTrials.gov