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N/A Completed N=21 Randomized Single-blind Treatment

Gene Expression Study Between Two Dermal Injectables Hydroxylapatite Semi-permanent Filler

Gene Expression
Source: ClinicalTrials.gov NCT05620043 ↗
Enrolled (actual)
21
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcomePrimary: Gene Expression — 1; 1; 1; 4 Significantly upregulated genes

Summary

To compare gene expression stimulated by a semi-permanent filler and a biostimulator via punch biopsy

Outcome Measures

OutcomeResultp-value
PRIMARY
Gene Expression
1; 1; 1; 4; 2; 2

Eligibility Criteria

Inclusion Criteria

  • Subject with a minimum of shallow nasolabial fold (NLF) contour deficiencies as assessed via the wrinkle assessment scale
  • Subject with identical WAS scores on both NLFs
  • Ability of giving consent for participation in the study
  • Agreement to have skin biopsies on NLFs

Exclusion Criteria

  • Significant NLF asymmetry, or different WAS score on each NLF
  • Pregnant, planning pregnancy during the course of the study or breastfeeding
  • History of allergy or hypersensitivity to any ingredient of the treatment products
  • History of allergy or hypersensitivity to anesthetics or lidocaine
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05620043). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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