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Not yet recruiting NCT07684222

Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring

No phase Interventional Radar Surgical Procedures, Operative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Radar-based non-contact cardiac function monitoring..
Who it may be relevant to
Registry conditions: Radar, Surgical Procedures, Operative. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Development of a Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring System for Preoperative and Postoperative Assessment in Surgical Patients

Overview

This research will develop and clinically validate a system that enables continuous and non-invasive monitoring of cardiac function in surgical patients during the pre- and post-operative periods using contactless radar sensor technology, within the scope of medical device development and clinical validation.

Interventions

  • Device Radar-based non-contact cardiac function monitoring.
    Development and clinical validation of a millimeter wave radar-based non-contact cardiac function monitoring system for preoperative and postoperative evaluation in surgical patients.

Primary outcome measures

  • Monitoring patients' cardiac function with medical devices-Heart rate [Time frame: 3 months]
  • Monitoring patients' cardiac function with medical devices-Respiratory rate [Time frame: 3 months]
  • Monitoring patients' cardiac function with medical devices-Blood pressure [Time frame: 3 months]
  • Monitoring patients' cardiac function with medical devices-Chest wall microvibrations [Time frame: 3 months]
  • Monitoring patients' cardiac function with medical devices-Stroke volume [Time frame: 3 months]
  • Monitoring patients' cardiac function with medical devices-cardiac output estimations [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Patients scheduled for cardiovascular surgery
  • Patients who volunteered to participate in the study.

Exclusion criteria

  • Patients with a body mass index <18 kg/m² or >30 kg/m²
  • Patients with known cardiac arrhythmias
  • Patients with severe pulmonary edema
  • Patients who wish to terminate their participation during the study period

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Screening

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07684222 · 55754-2 TUSEB

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗