Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections

T

The New York Eye & Ear Infirmary

Status

Completed

Conditions

Wrinkles
Rhytids

Treatments

Device: hyaluronic acid or calcium hydroxylapatite filler

Study type

Observational

Funder types

Other

Identifiers

NCT01034956
09.27

Details and patient eligibility

About

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.

Full description

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.

Enrollment

20 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Trial design

20 participants in 1 patient group

Facial Soft Tissue Filler Patients
Description:
Patients previously treated by Principal Investigator with facial soft tissue fillers within the past 2 years
Treatment:
Device: hyaluronic acid or calcium hydroxylapatite filler

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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