Sculptra Chart Review

Completed

• Conditions: Non-facial Skin Aesthetic Conditions
• Interventions: Device: Sculptra Aesthetic

• Registration Number: NCT05463978
• Lead Sponsor: Galderma R&D

Brief Summary

Multi-center retrospective chart review to evaluate the safety of Sculptra Aesthetic when used in non-facial areas

Detailed Description

Not available

Study Timeline

• Study Start: 2022-07-14
• Study First Submitted: 2022-07-14
• Study First Submitted QC: 2022-07-14
• Study First Posted: 2022-07-19
• Status Verified: 2022-09
• Primary Completion: 2022-10-14
• Study Completion: 2022-10-14
• Last Update Submitted: 2022-10-21
• Last Update Posted: 2022-10-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 500

Inclusion Criteria

• Subjects who have been treated at the site with Sculptra Aesthetic in non-facial areas
• Subjects with available information about treatment dates and treatment procedures

Exclusion Criteria

• Subject that have actively asked not to be involved in a study or registry
• Other conditions that in the Investigator's opinion would exclude the subject from participation ; the condition should be recorded.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Females/Males treated with Sculptra Aesthetic in non-facial areas	Sculptra Aesthetic	Sculptra Aesthetic administration in non-facial areas

Primary Outcome Measures

Name	Time	Method
To evaluate safety of Sculptra Aesthetic when used in non-facial areas	January 2018 to 2022	AEs related to the product or injection procedure reported in the medical chart

Trial Locations

Locations (2)

Site Coordinator; 🇺🇸 New York, New York, United States

Galderma Research Site; 🇺🇸 New York, New York, United States