Safety and Efficacy of Ellacor® Micro-coring® Following Best Practices on Technique and Post-Procedural Care

Part of paid clinical trials in Miami, Florida.

Sponsor
Cytrellis Biosystems, Inc.
Study ID
NCT07260578
Status
Enrolling By Invitation

Conditions

  • Best Practices
  • Ellacor
  • Ellacor Post Care
  • Micro-coring Post Care

Eligibility Criteria

Sex
ALL
Age
45 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

  • ellacor Micro-Coring Technology — DEVICE
    ellacor will be used to treat moderate-severe wrinkles in the mid to lower face in subjects aged between 45-65.

Study Details

Since its inception of being marketed in the United States in 2021, physicians have used various post procedure skin care regimen to facilitate recovery. This study aims to examine the use of three post care products in five skin care regimens

Key Dates

Start date
Nov 26, 2025
Status verified
Nov 2025
Primary completion
May 31, 2026
Completion
Jun 30, 2026

Study Design

Enrollment
24 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Active Comparator: Regenerating Skin Nectar (by Alastin) + Tegaderm
    Alastin to be applied post procedure followed up Tegaderm. Tegaderm will be left on for 12 hours. Alastin will be applied twice daily for the duration of the study
  • Active Comparator: Kerra+ Recovery Cream (by Quthero) + Tegaderm
    Patients will receive Kerra+ post procedure followed by Tegaderm. The Tegaderm is removed after 12 hours. Kerra+ will be applied twice daily for the duration of the study.
  • Active Comparator: Ariessence Platelet-Derived Growth Factor (PDGF) solution +Alastin + Tegaderm
    Patients will receive PDGF immediately post procedure followed by Alastin followed by Tegaderm. The Tegaderm will be removed after 12 hours and the Alastin will continue to be applied twice daily for the duration of the study
  • Active Comparator: Ariessence PDGF solution + Kerra+ Recovery Cream + Tegaderm
    Patients will receive PDGF immediately post procedure followed by Kerra+ followed by Tegaderm. The Tegaderm will be removed after 12 hours and the Kerra+ will continue to be applied twice daily for the duration of the study
  • Active Comparator: Tegaderm Only
    Patient will only receive Tegaderm for post-care

Primary Outcome Measure

Global Aesthetic Improvement Scale (GAIS) [ Time Frame: GAIS Assessment will be performed under a timeframe of 90 days ]

Locations (2)

FacilityCityStateZIPSite coordinators
Miami Dermatology And Laser InstituteMiamiFlorida33173-
Caloaesthetics Plastic Surgery CenterLouisvilleKentucky42022-

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