Monitoring

9

Review clinical trials related to Monitoring. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Non-contact Patient Monitoring With Millimeter Wave Radar Technology.

This study aims to develop a millimeter wave radar technology-based patient monitoring system that allows for the monitoring of physiological and movement-based data in healthcare settings without requiring physical contact with individuals. The study will involve the creation of hardware and software components for processing, analyzing, and converting signals obtained through radar sensors into clinically meaningful data.

Participants needed: 6
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Rukiye KokkizUpdated: Jul 1, 2026
Eligibility criteria

Participating in the research as a researcher

Wanting to withdraw from the research

Status: Not yet recruiting

Portrait Mobile Monitoring Solution V2.0 External Evaluation

The purpose of this study is to collect and assess feedback from the users regarding the functionality and performance of the Portrait Mobile Monitoring Solution V2.0. In addition, this study aims to collect raw parameter data from the investigational devices for use in current and future Portrait Mobile development, including engineering purposes as deemed appropriate by the Sponsor.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: GE HealthcareUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Participant is age 18 years or older (≥18 years). [+3]

Known to be pregnant and/or breast feeding. [+4]

Status: Recruiting

ESOTIP-TEE: Defining an Easy Landmark to Guide Correct Esophageal Probe Placement With Transesophageal Echocardiography

This prospective observational study aims to identify simple external anatomical landmarks that allow reliable prediction of correct esophageal probe insertion depth. Accurate placement in the lower third of the esophagus is essential for reliable core temperature monitoring. Transesophageal echocardiography (TEE) will be used as the reference standard to confirm correct probe position. The study will evaluate the agreement between landmark-based insertion depth and TEE-confirmed placement in adult ICU patients undergoing clinically indicated TEE.

Participants needed: 30
Trial details
Biological sex: AllType: ObservationalSponsor: Institute of Mountain Emergency MedicineUpdated: May 8, 2026Locations: 1
Eligibility criteria

Adult (≥18 years) patients admitted to the ICU [+1]

<18 years

Status: Recruiting

Correlation Between Capillary Refill Time and Perfusion Index in Critically Ill Patients

Assessment of capillary refill time (CRT) is a cornerstone of tissue perfusion monitoring in critically ill patients. CRT measurement is performed by applying brief and gentle pressure (for a few seconds) to a small area of skin until blanching occurs. CRT is defined as the time, in seconds, required for the skin surface to return to its initial color after release of pressure. Although CRT is a monitoring tool used on a daily basis in emergency departments and critical care units, its practical measurement modalities remain poorly standardized and time-consuming. Consequently, there is no consensus regarding the most reproducible bedside method for CRT assessment. Moreover, repeated CRT measurements during patient management are resource-intensive in terms of medical time and may raise issues related to healthcare staff availability. The perfusion index (PI) is a marker of tissue perfusion derived from a pulse oximetry sensor. This monitoring device is routinely used in all critically ill patients. It is placed on the finger and worn continuously, including during patient transport. Because PI measurement is automatic and continuous, establishing its correlation with CRT could allow for more precise tissue perfusion monitoring while reducing the time burden associated with bedside assessments in critically ill patients.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hospices Civils de LyonUpdated: May 1, 2026Locations: 2
Eligibility criteria

Adult patient. [+2]

Legal guardianship, curatorship, or judicial protection. [+2]

Status: Recruiting

The Use of the Bambi-Belt in Exteremly Preterm Infants: an Implementation Study.

This observational, non-interventional cohort study evaluates the clinical use of the Bambi Belt-a CE-certified, wireless device for non-invasive heart rate and respiration monitoring-in extremely preterm infants (\<26 weeks gestation). 15 infants with intact skin and age \<24 hours will be monitored using the Bambi Belt during the first ten days of life. Primary outcomes include ease of use (application, signal stability), skin tolerance, and user experience (nurses and parents). Standard care remains unchanged. Data will be collected via clinical records and evaluation forms.

Participants needed: 15
Trial details
Age: Up to 1Biological sex: AllType: ObservationalSponsor: Maxima Medical CenterUpdated: Mar 11, 2026Locations: 2Duration: 1 Month
Eligibility criteria

Not listed

Status: Not yet recruiting

Comparison of Hemodynamic Variables Between Using Conventional Invasive Catheter Monitoring and Non-invasive Piezoelectric Sensor

Arterial pressure is obtained from invasive arterial monitoring and noninvasive arterial monitoring using piezoelectric sensor and compared.

Participants needed: 30
Trial details
Age: 19+Biological sex: AllType: InterventionalSponsor: SMG-SNU Boramae Medical CenterUpdated: Aug 7, 2025
Eligibility criteria

Cases who require Invasive arterial pressure monitoring d/t bleeding.

Patients with cardiovascular disease, cerebrovascular diseases, renal disease, o... [+1]

Status: Not yet recruiting

Feasibility Study: Continuous Fetal Monitoring During Maternal Exercise

This feasibility study will be the first study to assess the feasibility of continuous electrophysiological monitoring during maternal exercise in women with an uncomplicated pregnancy. This may help to better understand fetal condition during exercise and offer personalised exercise recommendations in the future. In future, validating the feasibility and safety of exercise could promote greater exercise engagement among pregnant women and increase fetal wellbeiing.

Participants needed: 15
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Maxima Medical CenterUpdated: Jul 28, 2025
Eligibility criteria

Minimal age of 18 years old [+27]

Status: Recruiting

Correlation Between Noninvasive Blood Vessel Functionality Parameters and Cerebral Hemodynamics in Neurocritical Care Patients

The purpose of this clinical research project is to employ Mespere LifeSciences NeurOs Cerebral Oximetry system, equipped with noninvasive sensors approved by the FDA, to monitor and investigate the correlation within a cohort of patients suffering from traumatic brain injury (TBI), stroke, brain tumor, and brain bleeding. This study aims to investigate and establish the correlation between blood vessel functionality parameters-specifically, Vasodilation/Constriction Index (VDC), Vascular Resistance Index (VR), and Volume Reactivity Index (VRx)-with the crucial physiological indicators, Intracranial Pressure (ICP) and Mean Arterial Pressure (MAP). By doing so, the investigators seek to address fundamental questions surrounding cerebral hemodynamics and autoregulation in various neurological conditions.

Participants needed: 25
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of LouisvilleUpdated: May 30, 2025Locations: 1
Eligibility criteria

Adults (> 18 years of age); [+4]

Expected to be at increased risk due to study participation (e.g. due to hemodyn... [+5]

Status: Recruiting

Correlation Between Sedation Depth Monitoring and Reflexes During Intravenous Anesthesia With Dexmedetomidine and Remifentanil in Children Undergoing Direct Laryngoscopy for Surgical Procedures

This study evaluates the correlation between sedation depth monitoring obtained by NeuroSENSE ® NS 701 Monitor and reflexes during intravenous anesthesia in children undergoing direct laryngoscopy for surgical procedures.

Participants needed: 10
Trial details
Age: 1-8Biological sex: AllType: ObservationalSponsor: University Hospital, AntwerpUpdated: Jan 22, 2025Locations: 1
Eligibility criteria

Not listed