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Completed Not applicable Interventional Accepts healthy volunteers

Core Study of the Safety and Effectiveness of IDEAL IMPLANT(R) Saline-filled Breast Implants

ClinicalTrials.gov ID: NCT00858052

Public ClinicalTrials.gov record NCT00858052. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 10:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Core Study of the Safety and Effectiveness of IDEAL IMPLANT(R) Saline-filled Breast Implants in Women Who Are Undergoing Primary Breast Augmentation or Replacement of Existing Augmentation Implants

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to determine the safety and effectiveness of the IDEAL IMPLANT in women who are undergoing primary breast augmentation or replacement of existing saline-filled or silicone gel-filled augmentation implants.

Study identification

NCT ID
NCT00858052
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Ideal Implant Incorporated
Industry
Enrollment
500 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2009 (Actual)
Primary completion
Feb 2012 (Actual)
Completion
May 2021 (Actual)
Last update posted
Sep 30, 2021

2009 – 2021

United States locations

U.S. sites
24
U.S. states
4
U.S. cities
24
Facility City State ZIP Site status
Not listed Beverly Hills California — —
Not listed Folsom California — —
Not listed Huntington Beach California — —
Not listed Modesto California — —
Not listed Riverside California — —
Not listed Sacramento California — —
Not listed Santa Monica California — —
Not listed Stockton California — —
Not listed Boca Raton Florida — —
Not listed Boynton Beach Florida — —
Not listed Fort Lauderdale Florida — —
Not listed Hollywood Florida — —
Not listed Jacksonville Florida — —
Not listed Loxahatchee Groves Florida — —
Not listed Miami Florida — —
Not listed Ponte Vedra Beach Florida — —
Not listed Duluth Georgia — —
Not listed Marietta Georgia — —
Not listed Roswell Georgia — —
Not listed Allen Texas — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Irving Texas — —
Not listed Southlake Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00858052, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 30, 2021 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00858052 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →