Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections

Purpose of the study:

The overall goal of this study is to better understand patient experience with injectable facial fillers so that the investigators may provide the best results for their patients. To do this, the investigators are administering surveys to approximately 50 patients who have been treated by Dr. Anthony P Sclafani, MD, FACS.

Participation:

Participants will be asked to complete a brief questionnaire regarding their most recent treatment by Dr. Sclafani with a facial injectable filler. All responses will be analyzed anonymously.

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Key information

Conditions

Rhytids Behavior Health Behavior Patient Satisfaction Treatment Adherence and Compliance Wrinkles

Sex eligibility

All sexes

Study type

Observational

Primary location

The New York Eye & Ear Infirmary

New York, 10003, United States

About this study

Patients previously treated by the PI with dermal fillers will be mailed questionnaires about their experience with the treatment. These questionnaires will be deidentified prior to recording answers on a computer based spreadsheet.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients treated by Principal Investigator with facial soft tissue filler within the past 2 years willing to complete the research survey.

Exclusion criteria

Any patient not treated by Principal Investigator with facial soft tissue filler within the past 2 years.

Treatment and study plan

hyaluronic acid or calcium hydroxylapatite filler

Device

Intradermal and subdermal injection of facial soft tissue filler within the past 24 months; survey of patients to assess satisfaction and determine the presence of treatment related adverse events.

Other names: Restylane, Perlane, Juvederm, Radiesse

Primary outcomes

Satisfaction with treatment with facial soft tissue fillers

Time frame: 0-24 months

Secondary outcomes

Social and behavioral effects of facial soft tissue filler treatment

Time frame: 0-24 months

Sponsors and collaborators

Lead sponsor

The New York Eye & Ear Infirmary

Other

Collaborators

Thomas Jefferson University

Registry information

Important dates

Study start: 2009
Primary completion: 2010
Study completion: 2010
First posted: Dec 18, 2009
Registry last updated: May 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed