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NCT01708434 · ClinicalTrials.gov registry record · NA

Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees

A NA study, sponsored by Ulthera.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT01708434: Completed NA study, sponsored by Ulthera.

NCT01708434 is a NA study that has completed, run by Ulthera. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01708434, a NA study, has completed, sponsored by Ulthera.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

Enrolled subjects will receive one bilateral Ulthera® treatment on the knees. Up to 30 subjects will be enrolled. Study photos will be obtained prior to study treatment, immediately following study treatment, and at each post-treatment follow-up visit. Follow-up visits will occur at 90 and 180 days post-treatment.

Primary Outcome

Assessed based on Principal Investigator assessment using the Global Aesthetic Improvement Scale.

Interventions

  • DEVICE Ulthera® System

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2011-06
Est. Completion 2012-08
Phase NA
Ulthera

42 total trials

What the finished NCT01708434 record still lists

NCT01708434 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Ulthera® System is the first listed.

NCT01708434 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01708434 about?

NCT01708434 is a clinical study titled "Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees". Enrolled subjects will receive one bilateral Ulthera® treatment on the knees. Up to 30 subjects will be enrolled. Study photos will be obtained prior to study treatment, immediately following study treatment, and at each post-treatment follow-up visit. Follow-up visits will occur at 90 and 180 days ...

What is the current status of trial NCT01708434?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2011-06. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01708434?

The interventions under investigation include: Ulthera® System (DEVICE).

Who is sponsoring clinical trial NCT01708434?

This trial is sponsored by Ulthera, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01708434's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 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 NCT01708434, the US trial registry maintained by the National Library of Medicine. NCT01708434 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.