Lumenis Be

20 total trials 1 currently recruiting 15 completed

Lumenis Be sponsors 20 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 15 completed. The most-studied condition in this pipeline is Dry Eye Syndromes, with 1 trials.

Trial Pipeline

20 total, page 1 of 1

RECRUITING NA

Clinical Study to Evaluate the Improvement in Hair Loss in Skin of Color Treated With Fractional Non-Ablative Laser

NCT06885112

NOT YET RECRUITING NA

Evaluation of Effectiveness and Safety of Intense Pulsed Light Treatment for Chalazion

NCT07405138

TERMINATED NA

Evaluation of Effectiveness and Safety of Intense Pulsed Light Treatment for Chalazion

NCT07039461

COMPLETED NA

Feasibility of Dynamic Muscle Stimulation + Radiofrequency for Improving Blink Quality in Subjects with Dry Eye Disease

NCT05945069

COMPLETED NA

Evaluation of Thermal Outcome and Safety of Nuera Tight RF System

NCT05957029

COMPLETED NA

Safety and Efficacy Evaluation of SMART Camera Treatment Presets for Cutaneous Lesions Using IPL

NCT05755139

COMPLETED NA

Feasibility of IPL Combined With RF for Treatment of DED Due to MGD

NCT05487547

COMPLETED NA

Safety of Tinted Soft Scleral Eye Shields When IPL is Applied on Eyelids

NCT05168670

COMPLETED NA

Evaluation of the Immediate Effect and Safety of DMA™ Novel Muscle Stimulation Technology

NCT04296201

COMPLETED NA

Evaluation of the Safety and Efficacy of the NuEra Tight for Abdominal Circumference Reduction

NCT04406935

COMPLETED NA

Effectiveness of Intense Pulsed Light for Improving Dry Eye Syndrome

NCT03396913

COMPLETED NA

Feasibility of IPL for Reducing Dry Eye Symptoms Caused by MGD

NCT02621593

TERMINATED NA

Impact of the M22-IPL Acne Filter on Acne Vulgaris

NCT02180282

COMPLETED NA

Impact of M22 Synergistic Sequential Treatment (SST)

NCT02032771

COMPLETED NA

Impact of Synergistic Sequential Treatment (SST)

NCT01940445

COMPLETED NA

Clinical Evaluation of LightSheer Duet 805nm HS Handpiece

NCT01801202

TERMINATED NA

Scar Prevention Using Fractional Carbon Dioxide Laser Treatment

NCT01826942

COMPLETED NA

Clinical Evaluation of M22 ResurFX 1565nm Module

NCT01796626

COMPLETED NA

Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece

NCT01282866

COMPLETED

Evaluation of the LightSheer HS Hand Piece as Compared to the LightSheer ET Hand Piece for the Intended Use of Hair Removal and Permanent Hair Reduction

NCT00657085

Therapeutic Areas

What the Pipeline for Lumenis Be Shows

According to the ClinicalTrials.gov registry, Lumenis Be is linked to 20 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 5% of the sponsor's indexed portfolio, and 15 are already marked complete, representing roughly 75% of the total.

The phase mix for Lumenis Be 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 Lumenis Be is Dry Eye Syndromes 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.