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NCT01205061 · ClinicalTrials.gov registry record · NA

Emervel® Deep Lidocaine vs. Juvederm® Ultra Plus in Treatment of Moderate to Severe Facial Wrinkles and Folds

A NA study, sponsored by Galderma R&D.

Completed
Registry status
NA
Development phase
162
Enrollment target

NCT01205061: Completed NA study, sponsored by Galderma R&D.

NCT01205061 is a NA study that has completed, run by Galderma R&D. The registered enrollment target is 162 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01205061, a NA study, has completed, sponsored by Galderma R&D.

COMPLETED
Registry status
NA
Development phase
162 participants
Enrollment target

Study Summary

The purpose of the study was to compare the effectiveness and safety of Emervel Deep Lidocaine versus Juvederm Ultra Plus in the treatment of moderate to severe facial wrinkles and folds.

Primary Outcome

WSRS is a validated 5-point reference scale with photographs that classifies deep facial wrinkles (nasolabial folds). WSRS represents clinically meaningful change in NLF severity from the adjacent grades where 1= absent (no visible fold; continuous skin line), 2 = mild (shallow but visible fold with a slight indentation; minor facial feature; implant expected to produce a slight improvement in appearance), 3 = excellent (correction is expected from injectable implant), 4 = severe (very long and

Interventions

  • DEVICE Emervel Deep Lidocaine
  • DEVICE Juvederm Ultra Plus

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2010-09-27
Est. Completion 2012-01-12
Phase NA
Galderma R&D

158 total trials

What the finished NCT01205061 record still lists

NCT01205061 is an interventional study that assigns participants to a tested intervention. The registered 162 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 (88% lower).

The record links to 0 conditions, and to 2 interventions - of which Emervel Deep Lidocaine is the first listed.

NCT01205061 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01205061 about?

NCT01205061 is a clinical study titled "Emervel® Deep Lidocaine vs. Juvederm® Ultra Plus in Treatment of Moderate to Severe Facial Wrinkles and Folds". The purpose of the study was to compare the effectiveness and safety of Emervel Deep Lidocaine versus Juvederm Ultra Plus in the treatment of moderate to severe facial wrinkles and folds.

What is the current status of trial NCT01205061?

This trial is currently completed. It is a NA study. The enrollment target is 162 participants. The study started on 2010-09-27. Estimated completion is 2012-01-12.

What interventions are being tested in trial NCT01205061?

The interventions under investigation include: Emervel Deep Lidocaine (DEVICE), Juvederm Ultra Plus (DEVICE).

Who is sponsoring clinical trial NCT01205061?

This trial is sponsored by Galderma R&D, which has 158 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01205061's enrollment target sits among peer trials

162 627th of 2000 higher than 1,373 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 NCT01205061, the US trial registry maintained by the National Library of Medicine. NCT01205061 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.