CynosureLutronic
CynosureLutronic sponsors 9 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 5 completed. The most-studied condition in this pipeline is Benign Pigmented Lesions, with 1 trials.
Trial Pipeline
9 total, page 1 of 1
A Clinical Study to Evaluate the Efficacy and Safety of Ultra in Promoting Hair Regrowth
NCT07588243
Pilot Evaluation of the Lutronic PicoPlus System for the Treatment of Benign Pigmented Lesions of the Hands
NCT04208100
LaseMD System for the Treatment of Melasma
NCT03456674
Safety and Efficacy Evaluation of the Xerf Device for Aesthetic Treatments
NCT07585591
Safety and Efficacy of Electronic Stimulation for Circumferential Reduction and Muscle Toning
NCT06152900
Lutronic Genius System for Neck Treatment
NCT03534609
Lutronic Infini and LaseMD Systems in Combination Treatment
NCT03409965
Lutronic LaseMD for Treatment of Benign Pigmented Lesions
NCT03409952
Lutronic PicoPlus Exploratory Clinical Trial
NCT03415685
Therapeutic Areas
What the Pipeline for CynosureLutronic Shows
According to the ClinicalTrials.gov registry, CynosureLutronic is linked to 9 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 11% of the sponsor's indexed portfolio, and 5 are already marked complete, representing roughly 56% of the total.
The phase mix for CynosureLutronic 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 CynosureLutronic is Benign Pigmented Lesions with 1 linked trial, and 1 other condition area 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.