NCT04509089

Establishing Correlation Between Non-invasive Pulmonary Blood Pressure Readings and Swan-Ganz Results

Suremedix Ltd·ClinicalTrials.gov·device·Device trialCompleted
View on ClinicalTrials.gov
Study focus
Disease/Condition
Congestive Heart Failure
Drug/Device/Intervention
Suremedix Device
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Suremedix Ltd
Location
Petah Tikva, Israel
Timeline & enrollment
Phase
N/A
Start date
Dec 01, 2020
End date
Mar 01, 2021
Enrollment
15 participants
Primary outcome

Pressure waveform

Summary

Pulmonary hypertension (PH) is prognostic indicator in heart failure patients for poor
 outcome, however, it is challenging for monitoring. The current study is designed to explore
 whether data generated using Suremedix Device including a pump and non-invasive sensors
 including, chest motion sensor, photoplethysmography (PPG), and Electrocardiography (ECG),
 can be used to identify detectable oscillations that are correlated with the mean, the
 diastolic and the systolic pressure values of the pulmonary artery, as measured using the
 gold-standard Swan-Ganz method.

ICD-10 classifications
Congestive heart failureHeart failureHypertensive heart disease with (congestive) heart failureHypertensive heart and renal disease with (congestive) heart failureHeart failure, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04509089
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT04509089 through Pure Global AI's free database. This phase not specified trial is sponsored by Suremedix Ltd and is currently Completed. The study focuses on Congestive Heart Failure. 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.