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A Study to Evaluate the Long-term Safety and Effectiveness of Sculptra™

Recruitingn/aAges 18 Years - anyAllGalderma R&D
NCT07891767 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This is a non-interventional, multi-center, study designed to evaluate the long-term safety and effectiveness of Sculptra™ for the correction of midface volume deficit and/or midface contour deficiency in subjects of Chinese origin in standard clinical practice.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Men or women aged 18 years or older of Chinese origin. 2. Subjects who, independently of this study, received initial Sculptra treatment in the midface, with or without other facial areas, 11-12 months before screening, with relevant treatment records retained by the clinic. Exclusion Criteria: 1. Received any other sort of hyaluronic acid fillers and collagen-based filler in the midface within 1 year after the first Sculptra treatment in the midface. 2. Received treatment with semi-permanent filler in the midface within 1 year before the first Sculptra treatment in the midface up to Day 1. 3. Received treatment with permanent filler in the midface. 4. Participation in any other clinical study within 30 days before Day 1.
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What it tests

  • Not listed
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Where

1 site
Dermatology Hospital of Southern Medical University
Guangzhou, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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