RadarNCT07684222
Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring
A study testing Radar-based non-contact cardiac function monitoring. in people with Radar and Surgical Procedures, Operative, run by Rukiye Kokkiz.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Radar, Surgical Procedures, Operative
- What is being tested?
- Radar-based non-contact cardiac function monitoring.
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2026to 1 Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients scheduled for cardiovascular surgery
- Patients who volunteered to participate in the study.
Who cannot join
- 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
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Development of a Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring System for Preoperative and Postoperative Assessment in Surgical Patients
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
- Being tested
- Radar-based non-contact cardiac function monitoring.
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
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.
| Study group | Role | What they receive |
|---|---|---|
| patient monitoring | Other | Patients' cardiac functions will be monitored using a radar system. Receives: Device: Radar-based non-contact cardiac function monitoring. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Monitoring patients' cardiac function with medical devices-Heart rate
The following parameter will be measured as cardiac function:
Heart rate
Measured: 3 months
Monitoring patients' cardiac function with medical devices-Respiratory rate
The following parameter will be measured as cardiac function:
Respiratory rate
Measured: 3 months
Monitoring patients' cardiac function with medical devices-Blood pressure
The following parameter will be measured as cardiac function:
Blood pressure
Measured: 3 months
Monitoring patients' cardiac function with medical devices-Chest wall microvibrations
The following parameter will be measured as cardiac function:
Chest wall microvibrations
Measured: 3 months
Monitoring patients' cardiac function with medical devices-Stroke volume
The following parameter will be measured as cardiac function:
Stroke volume
Measured: 3 months
Monitoring patients' cardiac function with medical devices-cardiac output estimations
The following parameter will be measured as cardiac function:
cardiac output estimations
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Jul 2026
- Study start1 Sep 2026 (estimated)
- Primary completion1 Oct 2026 (estimated)
- Study completion1 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for RadarStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Rukiye Kokkiz
- Sponsor type
- University, hospital or other
- Collaborators
- Health Institutes of Turkey
- Responsible party
- Sponsor-investigator, Rukiye Kokkiz, Fenerbahce University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07684222
- Sponsor's protocol ID
- 55754-2 TUSEB
- Status last verified
- Jun 2026
- First submitted
- 18 Jun 2026
- Last updated
- 6 Jul 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development of a Millimeter Wave Radar-Based Non-Contact Cardiac Function Monitoring System for Preoperative and Postoperative Assessment in Surgical Patients
- ClinicalTrials.gov ID
- NCT07684222
- Acronym / sponsor ID
- 55754-2 TUSEB
- Conditions
- Radar, Surgical Procedures, Operative
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- Rukiye KokkizUniversity, hospital or other
- Collaborators
- Health Institutes of Turkey
- Study start
- 1 Sep 2026 (estimated)
- Primary completion
- 1 Oct 2026 (estimated)
- Study completion
- 1 Dec 2026 (estimated)
- First posted
- 6 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| patient monitoring | Other | Device: Radar-based non-contact cardiac function monitoring.Patients' cardiac functions will be monitored using a radar system. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Patients scheduled for cardiovascular surgery
- Patients who volunteered to participate in the study.
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 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. | Device | patient monitoring |
Primary outcome
Monitoring patients' cardiac function with medical devices-Heart rate
Time frame: 3 months
The following parameter will be measured as cardiac function: Heart rate
Monitoring patients' cardiac function with medical devices-Respiratory rate
Time frame: 3 months
The following parameter will be measured as cardiac function: Respiratory rate
Monitoring patients' cardiac function with medical devices-Blood pressure
Time frame: 3 months
The following parameter will be measured as cardiac function: Blood pressure
Monitoring patients' cardiac function with medical devices-Chest wall microvibrations
Time frame: 3 months
The following parameter will be measured as cardiac function: Chest wall microvibrations
Monitoring patients' cardiac function with medical devices-Stroke volume
Time frame: 3 months
The following parameter will be measured as cardiac function: Stroke volume
Monitoring patients' cardiac function with medical devices-cardiac output estimations
Time frame: 3 months
The following parameter will be measured as cardiac function: cardiac output estimations
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A study testing Radar-based non-contact cardiac function monitoring. in people with Radar and Surgical Procedures, Operative, run by Rukiye Kokkiz.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 6 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact rukiye kökkız (+90 507 140 68 98, rky_kokkiz@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Monitoring patients' cardiac function with medical devices-Heart rate (time frame: 3 months). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Jul 2026.