Brow Enhancement Study

NCT ID: NCT01308593

Last Updated: 2013-01-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-03-31

Study Completion Date

2011-10-31

Brief Summary

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Investigation into brow aesthetics using Botox in Conjunction with Juvederm XC as evaluated by patient satisfaction

Detailed Description

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Conditions

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Brow Ptosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Juvederm XC

Juvederm XC

Group Type ACTIVE_COMPARATOR

Juvederm XC

Intervention Type DEVICE

Filler

Botox

Medication used to block neuromuscular transmission

Group Type ACTIVE_COMPARATOR

Botox

Intervention Type DRUG

26 units dosed one time

Interventions

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Juvederm XC

Filler

Intervention Type DEVICE

Botox

26 units dosed one time

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Men and women

Exclusion Criteria

* Persons who have not had Botox for months.
* Women who are pregnant, breastfeeding, or trying to get pregnant.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Skin Care and Laser Physicians of Beverly Hills

OTHER

Sponsor Role lead

Responsible Party

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Derek H. Jones, M.D.

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Skin Care and Laser Physicians of Beverly Hills

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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Brow Study 25856/1

Identifier Type: -

Identifier Source: org_study_id

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