Cynosure
Cynosure sponsors 49 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 41 completed. The most-studied condition in this pipeline is Acne Scars, with 3 trials.
Trial Pipeline
49 total, page 1 of 1
Feasibility Study to Collect and Assess Safety Data for a Radiofrequency Microneedling Device for Electrocoagulation and Hemostasis of Soft Tissues for Dermatologic Conditions
NCT05987319
Clinical Study to Evaluate Alexandrite Laser for the Treatment of Acne Scars
NCT04807179
Pilot Evaluation of the Cynosure Potenza™ System for Treatment of Cosmetic Dermatologic Skin Conditions
NCT05847530
Prospective Clinical Study to Assess Safety and to Collect Data on Radiofrequency Microneedling Device(s) For the Purpose of Evaluating Treatment on Skin
NCT06023303
Study To Evaluate The Safety And Efficacy Of The MyEllevate® Procedure
NCT05590039
Clinical Study To Evaluate Paired Treatment With An Alexandrite Laser And Radiofrequency Microneedling For Facial Aging
NCT05388604
Study To Assess Radiofrequency Diathermocontraction Device For Muscle Stimulation And The Treatment Of Abdominal Fat
NCT05388617
Post Market Usability Evaluation Of The PicoSure Pro Device
NCT05102617
Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device
NCT05254210
Post Market Study To Collect Efficacy Data For The Treatment Of Wrinkles With A Radiofrequency Device
NCT05096247
Study To Assess The Safety And Efficacy Of The Tempsure Flexsure Applicators For Abdominal Wrinkles
NCT04930705
Post Market Clinical Follow Up Study to Collect Additional Data and Imaging
NCT04881058
Post Market Study Using The Elite IQ Device
NCT04807205
Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging
NCT04880070
Histological Study to Assess Safety and Efficacy of the TempSure Firm for Non-Invasive Lipolysis
NCT04878172
Rollover Study to Evaluate Histological Results of Radiofrequency Device Treatments on the Flanks
NCT04881149
Histological Study on Safety and Efficacy of a RF Device Flexible Applicator for Non-Invasive Lipolysis
NCT04881175
Multi-Center Traditional Feasibility Study of Radiofrequency Device
NCT04584099
Multi-Center Pivotal Study of Radiofrequency Device
NCT04569253
Study To Assess A Radiofrequency Microneedling Device For Dermatologic Conditions
NCT05097157
Clinical Study To Assess The Safety, Parameters And Efficacy For Procedures Using A Radiofrequency Device
NCT05166824
Study for the RevLite Laser System for Facial Solar Lentigines
NCT02110108
Picosure Alexandrite Laser and Revlite Nd:Yag Laser for the Treatment of Unwanted Tattoos
NCT02110121
Picosure Alexandrite Laser for the Treatment of Unwanted Tattoos
NCT02110095
A Study of the RevLite Laser System for the Treatment of Refractory Mixed Type Melasma
NCT02110134
The Smartlipo Triplex 1440nm Wavelength Laser and the Sidelaze 800 Hand Piece for the Treatment of Facial Acne Scars
NCT02103816
Clinical Evaluation of the Picosure Laser for the Treatment of Unwanted Tattoos
NCT02103153
Evaluating the Safety and Efficacy of the Pico Laser With a Specialized Lens Array for the Treatment of Wrinkles
NCT02091102
Evaluation of the Safety and Efficacy of the Pico Laser With a Specialized Lens Array for the Treatment of Wrinkles
NCT02091089
Evaluation of the Picosure 755nm Alexandrite Laser With Lens Array for the Treatment of Acne Scars
NCT02103127
Clinical and Histological Evaluation of the Picosure 755nm Laser With Cap Array for Facial Rejuvenation
NCT02107157
Evaluation of the Safety and Precursors of Efficacy
NCT02098811
Combination Alexandrite Laser and Topical Therapy vs Topical Therapy Alone for Treatment of Melasma
NCT02095756
Evaluation of 1440nm Laser Assisted Selective Photothermolysis for Treatment of Axillary Hyperhidrosis
NCT02100072
Evaluation of the 755nm Alexandrite for Unwanted Tattoos
NCT01842815
Evaluation of the 755nm Alexandrite for the Treatment of Epidermal and Dermal Pigmented Lesions
NCT01754233
Evaluation of the 755nm Alexandrite Laser for Skin Toning and Epidermal Pigmented Lesions in Asian Skin Types
NCT01754246
Clinical and Histological Evaluation of the 755nm Alexandrite Laser With Handpiece for the Treatment of Scars
NCT01813786
Treatment of Periorbital and Perioral Wrinkles With the Applications of the Iluminage Diode Laser
NCT01813760
Evaluation of 1440nm Laser vs. Botulinum Toxin or miraDry® Microwave For Treatment of Axillary Hyperhidrosis
NCT01811004
Mandible and Sub-mandible Using the 1440nm Wavelength Laser and Hand Piece
NCT01813747
Revlite Laser System Compared to the Candela Alex TriVantage System Refractory Mixed Type Melasma
NCT01745224
Evaluation of the 755nm Alexandrite Laser for the Treatment of Scars
NCT01811030
Investigation of Hyperhidrosis Treatment Using the Nd: YAG 1440nm Wavelength Laser
NCT01810991
Clinical Investigation of Non Invasive Fat Reduction
NCT01842802
755nm Alex Laser for Treatment of Stretch Marks
NCT01745211
Evaluation of the 755nm Alexandrite Laser for the Treatment of Tattoos
NCT01754207
755nm Alex Laser for Treatment of Pigmented and Vascular Lesions and Scars
NCT01745627
Laser Treatment for Fresh Surgical Scars and Mature Scars
NCT01030198
What the Pipeline for Cynosure Shows
According to the ClinicalTrials.gov registry, Cynosure is linked to 49 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 2% of the sponsor's indexed portfolio, and 41 are already marked complete, representing roughly 84% of the total.
The phase mix for Cynosure reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Cynosure is Acne Scars with 3 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.