Loading clinical trials...
Loading clinical trials...
Low Frequency Therapeutic Ultrasound System Pivotal Clinical Trial
Multi-center randomized trial to assess the safety and performance of low-frequency therapeutic ultrasound for maintaining renal function after contrast exposure.
This is a multi-center, randomized, controlled clinical trial designed to assess the safety and performance of the Sonogenix RENOBOOST as an adjunctive therapy for maintaining renal function after contrast exposure. The trial will enroll up to 234 subjects not taking oral nitrates and at high-risk of developing PC-AKI undergoing coronary arteriography for a planned percutaneous coronary intervention in up to 10 clinical sites in the US and up to 3 clinical sites outside the US. All subjects will be pre- treated with 0.9 percent NaCl at 3 ml/kg/h 1 hour before and 1 ml/kg/h during and 6 hours post procedure. Participants will be randomized in a 2:1 fashion to either active adjunctive therapy with the Sonogenix RENOBOOST or sham control. Subjects will have clinical follow-up examination 30 days post index procedure.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Henry Ford Hopsital
Detroit, Michigan, United States
McLaren Northern Michigan
Petoskey, Michigan, United States
University of Pennsylvania Medical Center
Pittsburgh, Pennsylvania, United States
UT Health San Antonio
San Antonio, Texas, United States
Start Date
September 24, 2021
Primary Completion Date
January 23, 2023
Completion Date
January 23, 2023
Last Updated
April 12, 2023
2
ACTUAL participants
Low-frequency therapeutic ultrasound (LOTUS)
DEVICE
LOTUS System with Ultrasound Disabled
DEVICE
Lead Sponsor
Sonogenix
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07358572