Safety and Efficacy of Matrix Pro for Eyebrow Lift and Lift of Submental/Neck Laxity

Part of paid clinical trials in Marlborough, Massachusetts.

Sponsor
Candela Corporation
Study ID
NCT06640998
Status
Enrolling By Invitation

Conditions

  • Laxity; Skin

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Accepted

Interventions

  • Matrix Pro — DEVICE
    Study subjects received up to three (3) study treatments with the Matrix Pro applicator

Study Details

Prospective, non-randomized, multi-center, pivotal clinical trial

Key Dates

Start date
Sep 9, 2024
Status verified
Oct 2024
Primary completion
Sep 30, 2027
Completion
Sep 30, 2028

Study Design

Enrollment
150 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Zone 1: Eyebrow Lift
    Treatment of the upper face including treatment of forehead to mid cheek
  • Experimental: Zone 2: Submentum and Neck
    Treatment of the lower face including mid to low cheek, submentum, and neck

Primary Outcome Measure

Improvements in lifting of lax tissue [ Time Frame: 3 months post last treatment ]

Locations (1)

FacilityCityStateZIPSite coordinators
Candela Institute for ExcellenceMarlboroughMassachusetts01752-

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