Pure Global

Human Factors Testing for OTC Use of the Erchonia® LunulaLaser - Trial NCT05626270

Access comprehensive clinical trial information for NCT05626270 through Pure Global AI's free database. This phase not specified trial is sponsored by Erchonia Corporation and is currently Completed. The study focuses on Onychomycosis. Target enrollment is 15 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
Device Trial
NCT05626270
Completed
Device Trial
device
Trial Details
ClinicalTrials.govNCT05626270
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Human Factors Testing for OTC Use of the Erchonia® LunulaLaser
Human Factors Validation Testing for Over-the-Counter Use of the Erchonia® LunulaLaser™ OTC

Study Focus

Onychomycosis

LunulaLaser OTC

Interventional

device

Sponsor & Location

Erchonia Corporation

Melbourne, United States of America

Timeline & Enrollment

N/A

Jun 04, 2021

Dec 23, 2022

15 participants

Primary Outcome

Human Factors

Summary

Human factors validation testing to assess the intended user's ability to correctly, safely,
 and effectively set-up, activate and operate the LunulaLaser™ OTC, to administer a treatment
 to a suitably qualified client, and to understand the information contained in the Erchonia
 LunulaLaser™ OTC Installation and Proper Use Reference Guide and box labeling.

ICD-10 Classifications

Onychogryphosis
Chromomycosis, unspecified
Onycholysis
Actinomycosis
Blastomycosis

Data Source

ClinicalTrials.gov

NCT05626270

Device Trial