Xeomin, Radiesse, and Belotero Facial/Neck Rejuvenational

Part of paid clinical trials in Ardmore, Pennsylvania.

Sponsor
Main Line Center for Laser Surgery
Study ID
NCT05039723
Phase
PHASE4
Status
Completed

Conditions

  • Photoaging

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Accepted

Interventions

Study Details

The purpose of this study is to determine the improvement in signs of photoaging and subject satisfaction after combination, global facial and/or neck treatment with IncobotulinumA (Xeomin), HA (Belotero) and/or calcium hydroxyapatite (Radiesse+, Radiesse Classic). All products will be used on-label FDA-cleared indications.

Key Dates

Start date
Sep 1, 2021
Status verified
Jul 2022
Primary completion
Mar 1, 2022
Completion
Jul 1, 2022

Study Design

Enrollment
22 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Treatment
    Treatment with Xeomin, Radiesse, and/or Belotero

Primary Outcome Measure

FACE-Q Subject Satisfaction [ Time Frame: 3 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Main Line Center for Laser SurgeryArdmorePennsylvania19003-

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