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ENROLLING BY INVITATION
NCT06726122
NA

Clinical Study to Evaluate the Efficacy and Safety of Matrix Pro Treatment

Sponsor: Candela Corporation

View on ClinicalTrials.gov

Summary

This is a non-randomized, multi-center, open-label, prospective clinical trial evaluating clinical treatments with the Matrix Pro Applicator for the improvement of facial and/or submental and neck laxity.

Official title: Clinical Study to Evaluate the Efficacy and Safety of Matrix Pro Treatment for Facial, Submental and Neck Laxity

Key Details

Gender

All

Age Range

18 Years - 84 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-01-28

Completion Date

2028-05

Last Updated

2025-06-15

Healthy Volunteers

Yes

Interventions

DEVICE

Profound Matrix

Treatment visits are limited to up to three (3) study treatments (with treatment intervals 6 weeks ± 2 weeks).

Locations (3)

Kliniek voor Esthetische Geneeskunde

Amsterdam, EK, Netherlands

Illuminate Skin & Wellness Clinic

Kings Hill, Kent, United Kingdom

GHB Clinic

London, United Kingdom