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NCT01722916 Clinical Trial

Reducing and Removing Hyaluronic Acid Filler With Hyaluronidase

Drug Safety Clinical Trial

Official title:
Pilot Study of Appropriate Dosing for Reducing and Removing Hyaluronic Acid Filler With Hyaluronidase: A Randomized Control Clinical Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT01722916
Other study ID # STU68166
Secondary ID
Status Active, not recruiting
Phase Early Phase 1
First received
Last updated
Start date October 2012
Est. completion date December 2024

Study information
Verified date February 2024
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to find how much hyaluronidase should be used when receiving injections of fillers.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 5
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Age 18 and over - The subjects are in good health - The subject has the willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator Exclusion Criteria: - Under 18 years of age - Pregnancy or Lactation - Subjects who are unable to understand the protocol or to give informed consent - Subjects with mental illness - Recent Accutane use in the past 6 months - Subjects prone to hypertrophic and keloidal scarring - Subjects with tattoos and/or scars on upper medial arms (the treatment area) - Subjects with known hypersensitivity to hyaluronic acid

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Hyaluronidase

Locations
Country Name City State
United States Northwestern University Department of Dermatology Chicago Illinois

Sponsors (1)
Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Dose of hyaluronidase injected until the filler is no longer detectable 2 weeks
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