Micro-Coring® for the Treatment of Skin Laxity of the Knees

Part of paid clinical trials in Sacramento, California.

Sponsor
Cytrellis Biosystems, Inc.
Study ID
NCT07409090
Status
Enrolling By Invitation

Conditions

  • Body
  • Knees

Eligibility Criteria

Sex
ALL
Age
22 Years - 70 Years
Healthy Volunteers
Accepted

Interventions

  • Micro-Coring — DEVICE
    Non-thermal device

Study Details

Early, informal clinical experience suggests that Micro-Coring may help improve skin quality in certain body areas, such as the knees. However, this body region has not yet been formally studied. Additional clinical evaluation is needed to better understand healing, potential side effects, patient experience, ease of use, and optimal treatment settings for body sites. This is especially important because body skin differs from facial skin in thickness, blood supply, movement, and mechanical stress, which may affect both safety and healing outcomes.

Key Dates

Start date
Feb 2, 2026
Status verified
Jan 2026
Primary completion
Jun 30, 2026
Completion
Aug 31, 2026

Study Design

Enrollment
12 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Other: Micro-Coring on the knees
    ellacor as the micro-coring intervention

Primary Outcome Measure

Correct identification of before and after treatment photos [ Time Frame: 90 days ]

Locations (1)

FacilityCityStateZIPSite coordinators
Laser & Skin Surgery Center of Northern CaliforniaSacramentoCalifornia95816-

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