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Brow Enhancement Study

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01308593
First Posted: March 4, 2011
Last Update Posted: January 4, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Derek H. Jones, M.D., Skin Care and Laser Physicians of Beverly Hills
  Purpose
Investigation into brow aesthetics using Botox in Conjunction with Juvederm XC as evaluated by patient satisfaction

Condition Intervention Phase
Brow Ptosis Device: Juvederm XC Drug: Botox Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Investigation Into Brow Aesthetics Using Botox in Conjunction With Juvederm Ultra XC as Evaluated by Patient Satisfaction

Resource links provided by NLM:


Further study details as provided by Derek H. Jones, M.D., Skin Care and Laser Physicians of Beverly Hills:

Primary Outcome Measures:
  • Participant satisfaction with combined injection with Botox and Juvederm XC [ Time Frame: 5 months ]

Enrollment: 30
Study Start Date: March 2011
Study Completion Date: October 2011
Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Juvederm XC
Juvederm XC
Device: Juvederm XC
Filler
Active Comparator: Botox
Medication used to block neuromuscular transmission
Drug: Botox
26 units dosed one time

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01308593


Locations
United States, California
Skin Care and Laser Physicians of Beverly Hills
Los Angeles, California, United States, 90069
Sponsors and Collaborators
Skin Care and Laser Physicians of Beverly Hills
  More Information

Responsible Party: Derek H. Jones, M.D., Principal Investigator, Skin Care and Laser Physicians of Beverly Hills
ClinicalTrials.gov Identifier: NCT01308593     History of Changes
Other Study ID Numbers: Brow Study 25856/1
First Submitted: March 2, 2011
First Posted: March 4, 2011
Last Update Posted: January 4, 2013
Last Verified: January 2013

Additional relevant MeSH terms:
onabotulinumtoxinA
Acetylcholine Release Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Cholinergic Agents
Neurotransmitter Agents
Physiological Effects of Drugs