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Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections

Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01034956
Enrollment
20
Registered
2009-12-18
Start date
2009-11-30
Completion date
2010-05-31
Last updated
2012-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rhytids, Wrinkles

Keywords

Soft tissue filler, Dermal filler, Complications, Patient satisfaction

Brief summary

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.

Detailed 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.

Interventions

DEVICEhyaluronic acid or calcium hydroxylapatite filler

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.

Sponsors

Thomas Jefferson University
CollaboratorOTHER
The New York Eye & Ear Infirmary
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Satisfaction with treatment with facial soft tissue fillers0-24 months

Secondary

MeasureTime frame
Social and behavioral effects of facial soft tissue filler treatment0-24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026