Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring

NCT07684222 | Not Yet Recruiting

• 1 other identifier: 55754-2 TUSEB
• Study Type: interventional
• Target: 30
• Locations: 0 countries
• Sites: N/A

Brief Summary

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.

Conditions

Radar; Surgical Procedures, Operative

Outcome Measures

Primary Outcomes (6)

• Monitoring patients' cardiac function with medical devices-Heart rate

  The following parameter will be measured as cardiac function: Heart rate

  3 months

• Monitoring patients' cardiac function with medical devices-Respiratory rate

  The following parameter will be measured as cardiac function: Respiratory rate

  3 months

• Monitoring patients' cardiac function with medical devices-Blood pressure

  The following parameter will be measured as cardiac function: Blood pressure

  3 months

• Monitoring patients' cardiac function with medical devices-Chest wall microvibrations

  The following parameter will be measured as cardiac function: Chest wall microvibrations

  3 months

• Monitoring patients' cardiac function with medical devices-Stroke volume

  The following parameter will be measured as cardiac function: Stroke volume

  3 months

• Monitoring patients' cardiac function with medical devices-cardiac output estimations

  The following parameter will be measured as cardiac function: cardiac output estimations

  3 months

Study Arms (1)

patient monitoring

OTHER

Patients' cardiac functions will be monitored using a radar system.

Device: Radar-based non-contact cardiac function monitoring.

Interventions

Radar-based non-contact cardiac function monitoring. DEVICE

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

patient monitoring

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

• 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

Sponsors & Collaborators

• Rukiye Kokkiz: lead
• Health Institutes of Turkey: collaborator

Central Study Contacts

rukiye kökkız

CONTACT

+90 507 140 68 98; rky_kokkiz@hotmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SCREENING
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: LECTURER

Study Record Dates

• First Submitted: June 18, 2026
• First Posted: July 6, 2026
• Study Start (Estimated): September 1, 2026
• Primary Completion (Estimated): October 1, 2026
• Study Completion (Estimated): December 1, 2026
• Last Updated: July 6, 2026

Record last verified: 2026-06

Data Sharing

• IPD Sharing: Will not share