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Completed

NCT Number: NCT02613481

The Emotional and Functional Benefits of Poly-L-Lactic Acid

This study will evaluates the emotional and functional benefits of Poly-L-Lactic Acid (Sculptra™), a cosmetic product used to fill defects of the skin. All participants will receive Sculptra™.

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Key information

Conditions

Facial Volume Loss

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Facial volume loss can result in emotional distress and functional impairment in some affected individuals. Poly-L-Lactic Acid (Sculptra™) stimulates collagen production in the skin thereby replenishing some of the collagen lost to natural aging and ultraviolet damage. This study will assess the emotional and functional benefits of Poly-L-Lactic Acid treated subject's through self report measurement tools.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Subject must be an outpatient, male or female subjects of any race, 35 years of age or older.
  • Subject must have any degree of facial volume loss.
  • Subjects of all Fitzpatrick skin types are eligible.
  • Subject must be able to follow study instructions and likely to complete all required visits, as assessed by the Investigator.
  • Subject must sign an IRB-approved Informed Consent form, Photographic Release Form, and the Authorization for Use and release of Health and Research Study Information (HIPAA) form prior to any study-related procedures being performed.

Exclusion criteria

  • Any of the previous facial treatments:

c. Any facial filler in the past 2 years d. Prior injection of permanent facial implant

  • Have any skin pathology or condition that could interfere with the evaluation of the face.
  • Be unable to communicate or cooperate with the Investigator due to a language barrier (non-English speaking), poor mental development, or impaired cerebral function.
  • Have evidence of alcohol or drug abuse (Investigator opinion), or history of poor cooperation, non-compliance with medical treatment, or unreliability.
  • Have used an investigational device, biologic or drug in the past 30 days, or be currently participating in an experimental drug, biologic or device trial.
  • Have a condition or be in a situation that, in the Investigator's opinion, may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study.
  • Be an employee (or a relative of an employee) of the Investigator, Sponsor or representative of the Sponsor.

Treatment and study plan

Poly-L-Lactic Acid (Sculptra) injection

Drug

1 vial of of poly-l-lactic acid (Sculptra) reconstituted in the usual sterile fashion with 7cc of sterile water and 2cc of Lidocaine without epinephrine. The contents of the vial will be injected as deemed appropriate by the certified injector and agreed upon by the study subject.

Primary outcomes

  1. Mean Subject Self Reported Quality of Life Scale

    Time frame: 3 months post initial injection

    Self report Likert Scale Title: Facial Volume Restoration Outcome Questionnaire 35 Questions 1-7 rating with higher score meaning a worse outcome

  2. Mean Rosenberg Self-Esteem Scale

    Time frame: 3 months post initial injection

    Self reported self esteem measure Title: Rosenberg Self-Esteem Scale Scale of 1-4, scale design with higher score relating to worse outcome.

  3. Mean Rosenberg Self-Esteem Scale

    Time frame: 6 months post initial injection

    Self reported self esteem measure Title: Rosenberg Self-Esteem Scale Scale of 1-4, scale design with higher score relating to worse outcome.

  4. Mean Subject Self Reported Quality of Life Scale

    Time frame: 6 months post initial injection

    Self report Likert Scale Title: Facial Volume Restoration Outcome Questionnaire 35 Questions 1-7 rating with higher score meaning a worse outcome

Sponsors and collaborators

Lead sponsor

Yardley Dermatology Associates

Other

Collaborators

  • Galderma R&D

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Nov 24, 2015
Registry last updated
May 29, 2019

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.

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