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NCT01785069 · ClinicalTrials.gov registry record · NA

Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped, Silicone-filled X-Style and L-Style Breast Implants

A NA study, sponsored by Allergan.

Terminated
Registry status
NA
Development phase
355
Enrollment target

NCT01785069: Clinical Trial NA study, sponsored by Allergan.

NCT01785069 is a NA study that was terminated before completion, run by Allergan. The registered enrollment target is 355 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01785069, a NA study, was terminated before completion, sponsored by Allergan.

TERMINATED
Registry status
NA
Development phase
355 participants
Enrollment target

Study Summary

This is a prospective, multicenter study of the safety and effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped, Silicone-Filled X-Style and L-Style Breast Implants.

Primary Outcome

The investigator rated their satisfaction with the participant's breast implant for each breast on a 5-point scale (1=Definitely dissatisfied, 2=Somewhat dissatisfied,3=Neither satisfied or dissatisfied, 4=Somewhat satisfied, 5=Definitely satisfied). If there was a different response for the left and right breasts the worst response was used. The percentage of participants where the investigator responded: "Definitely satisfied" or "Somewhat satisfied" is reported.

Interventions

  • DEVICE Anatomically shaped, silicone-filled breast implants with low projection or extra-full projection

Trial Details

FieldValue
Enrollment Target 355 participants
Start Date 2012-12-10
Est. Completion 2015-11-30
Phase NA
Allergan

314 total trials

Why NCT01785069 stopped before completion

NCT01785069 is an interventional study that assigns participants to a tested intervention. The registered 355 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (75% lower).

The record links to 0 conditions, and to 1 intervention - of which Anatomically shaped, silicone-filled breast implants with low projection or extra-full projection is the first listed.

NCT01785069 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01785069 about?

NCT01785069 is a clinical study titled "Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped, Silicone-filled X-Style and L-Style Breast Implants". This is a prospective, multicenter study of the safety and effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped, Silicone-Filled X-Style and L-Style Breast Implants.

What is the current status of trial NCT01785069?

This trial is currently terminated. It is a NA study. The enrollment target is 355 participants. The study started on 2012-12-10. Estimated completion is 2015-11-30.

What interventions are being tested in trial NCT01785069?

The interventions under investigation include: Anatomically shaped, silicone-filled breast implants with low projection or extra-full projection (DEVICE).

Who is sponsoring clinical trial NCT01785069?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01785069's enrollment target sits among peer trials

355 291st of 2000 higher than 1,710 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01785069, the US trial registry maintained by the National Library of Medicine. NCT01785069 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.