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CLINICAL TRIALS, STUDIES, REGISTRIES, DATA

Perspectum Partners with UT Southwestern Medical Center on Dallas Heart & Minds Study

The DHMS initial aim was to improve the diagnosis, prevention and treatment of heart disease, over the years this has expanded to encompass metabolic diseases, such as fatty liver disease.  

Nevisense to Be Included in a Large Clinical Study Initiated by The Ronald O. Perelman Department of Dermatology Clinic at NYU Langone Health

The SpotCheck study will investigate the use of Nevisense as a point-of-care diagnostic tool to assist with skin cancer detection in a remote setting such as a non-specialist practice or pharmacy.

FDA IDE Approval to Initiate a Pivotal Study of the NEXUS Aortic Arch Stent Graft System Has Been Announced

Earlier this year, FDA granted NEXUS™ Aortic Arch Stent Graft System as a breakthrough device.

First Patient Enrolled in PATHFINDER I Registry

The PATHFINDER I Registry is a pilot study to evaluate the safety and efficacy of the Auryon Atherectomy System in the real-world treatment of de novo, re-stenotic, and in-stent restenosis lesions in infrainguinal arteries of patients with Peripheral Artery Diseases.

miR Scientific Notes Validation of its Urine Based, Non-Invasive Prostate Cancer Test Is Published in the Journal of Urology

MiR Scientific notes the data show that miR Scientific's platform can detect molecular evidence of prostate cancer with sensitivity of 94% and specificity of 92%, which translates to AUC of 0.98.

AuroLase ® Pivotal Study Update: Four Clinical Trial Sites Added Notes Nanospectra Biosciences

The AuroLase pivotal study follows the successful first-in-human pilot study that enrolled 46 subjects at three U.S. sites. Pandemic related delays to the one-year end of study biopsies for the final subset of feasibility study subjects should be resolved within the next several weeks and, consequently, final results of the feasibility study are expected later this year.

First Enrollments in the TactiFlex PAF IDE Study Underway

The study will evaluate the performance of the investigational TactiFlex™ Ablation Catheter, Sensor Enabled™ for people whose AFib symptoms are unable to be managed by medication.

MolecuLight Reports 10 Clinical Posters and Video Presentations at SAWC

"We are thrilled to have had a record number of MolecuLight-based clinical posters and presentations, from so many wound care professionals and settings, be included at the SAWC's Virtual Session", says Anil Amlani, MolecuLight's CEO.

Guided Therapeutics Submits Clinical Study Protocol to U.S. FDA for LuViva® Advanced Cervical Scan

LuViva will be studied to assess its ability to help detect a significant number of the up to 40% to 50% cases missed at the point of biopsy because of limitations in current imaging technology.