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Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections

NCT01034956 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2012-05-01

No results posted yet for this study

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.

Conditions

  • Rhytids
  • Wrinkles

Interventions

DEVICE

hyaluronic 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 & Collaborators

  • Thomas Jefferson University

    collaborator OTHER

  • The New York Eye & Ear Infirmary

    lead OTHER

Principal Investigators

  • Anthony P Sclafani, MD · The New York Eye & Ear Infirmary

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2010-03-31
Completion
2010-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01034956 on ClinicalTrials.gov