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NCT04680039

Early Warning of Intradialytic Hypotension in Hemodialysis Patients

Completed Last updated 20 July 2022
What this trial tests

trial testing Continuous monitoring in Hypotension of Hemodialysis in 150 participants. Completed in 15 March 2022.

Timeline
15 January 2021
Primary endpoint
15 February 2022
15 March 2022

Quick facts

Lead sponsorBiobeat Technologies Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment150
Start date15 January 2021
Primary completion15 February 2022
Estimated completion15 March 2022
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Biobeat Technologies Ltd.

Who can join

Adults 18 to 120, any sex, with Hypotension of Hemodialysis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this study, the investigators will monitor patients undergoing hemodialysis treatment with a non-invasive wearable PPG-based device. Measurements will include blood pressure, heart rate, oxygen saturation, stroke volume, cardiac output, cardiac index and systemic vascular resistance, among others. The aim is to diagnose intradialytic hypotension more rapidly than with current noninvasive methods and prevent related poor outcomes.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Continuous Monitoring of Advanced Hemodynamic Parameters during Hemodialysis Demonstrated Early Variations in Patients Experiencing Intradialytic Hypotension
    Kolben Y, Gork I, Peled D, Amitay S, et al · · 2024

Verify or expand the search:

Other recruiting trials for Hypotension of Hemodialysis

Currently open trials in the same condition.

Other Biobeat Technologies Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04680039.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing