Clinical trials: Vital Signs Monitoring
Surgery--Complications
Screening for Postoperative Vital Signs Abnormalities, and Particularly Hemodynamic Ones, by Continuous Monitoring Using the Biobeat Patch
Brief Summary: Post-operative morbidity remains a reality as shown by the International Surgical Outcomes Study published in 2016 and 2019 and by several recent publications which focus mainly on hypotension and cardio-vascular…
- Trial name
- Biobeat-Postop (NCT04585178)
- Testing
- Biobeat patch
- Where
- 2 sites in France
- Volunteers
- 109 people
- Sponsor
- Hopital Foch
Neonates and Preterm Infants, Infant Respiratory Distress Syndrome
Duration of Surfactant Administration and Impact on Stabilisation of Vital Parameters in Very Preterm Neonates: 1 Minutes Versus 5 Minutes
Respiratory distress syndrome (RDS) is common in very preterm infants due to surfactant deficiency. Surfactant replacement therapy is lifesaving, and current guidelines recommend the less invasive surfactant administration (LISA)…
- Conditions
- Neonates and Preterm Infants, Infant Respiratory Distress Syndrome, Surfactant Deficiency Syndrome Neonatal, Surfactant
- Trial name
- SurfStab I (NCT07261787)
- Testing
- Poractant alfa (Curosurf®) - 1-minute administration, Poractant alfa (Curosurf®) - 5-minute administration
- Where
- Austria
- Volunteers
- 76 people
- Sponsor
- Medical University of Graz
Other Preterm Infants
Monitoring of Vital Signs During Skin-to-skin Holding by Mothers of Their Preterm Babies
This observational study aims to monitor the vital sign changes in both mother and baby that occur during kangaroo care in preterm infants and to investigate any potential correlations between maternal measurement values and…
- Trial name
- NCT02231801
- Testing
- Mother-Infant Dyad
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Icahn School of Medicine at Mount Sinai
Vital Signs
Video Monitoring FOR Early Signaling of Adverse EvEnts, Technical Validation
In this study, 30 patients admitted to an high acuity department with hemodynamic or respiratory pathologies will be monitored with camera-based monitoring technologies for 24 hours.
- Trial name
- FORSEE (NCT05455775)
- Testing
- Camera-based monitoring technology
- Where
- Netherlands
- Volunteers
- 36 people
- Sponsor
- Catharina Ziekenhuis Eindhoven
Monitoring, Physiologic, Vital Signs
Bodytrak® Feasibility Study
Bodytrak® is a wireless earpiece which can monitor the user's vital signs such as tympanic (ear) temperature and heart rate. The earpiece is non-invasive and should fit comfortably within the right ear, similar to an earphone…
- Conditions
- Monitoring, Physiologic, Vital Signs, Sepsis, Altered Level of Consciousness
- Trial name
- NCT03139955
- Testing
- Bodytrak
- Where
- United Kingdom
- Volunteers
- 8 people, healthy volunteers welcome
- Sponsor
- Inova Design Solutions Ltd
Cancer, Cardiovascular Diseases
Telematics Device for Daily Monitoring of Vital Signs in Cancer
The primary goal of this non-profit single-centre randomized pilot interventional study is to evaluate the acceptability of a daily telemonitoring of five vital parameters (heart rate, respiratory rate, blood oxygenation, blood…
- Conditions
- Cancer, Cardiovascular Diseases, Respiratory Disease
- Trial name
- ButterfLife (NCT05650814)
- Testing
- ButterfLife, Control
- Where
- Italy
- Volunteers
- 50 people
- Sponsor
- Fondazione ANT Franco Pannuti ETS
Cancer, Emergencies
Pro-active Monitoring of Vital Signs in Oncology Patients Using a Smartwatch
The goal of this single center prospective observational study is to determine the effect of chemotherapy on (the change in) vital parameters.
- Trial name
- PROGRESS (NCT06680778)
- Testing
- Proactive Monitoring
- Where
- Netherlands
- Volunteers
- 175 people
- Sponsor
- Erasmus Medical Center
Body Temperature, Oxygen Saturation
Clinical Evaluation of the Vital Signs Monitoring System (VSMS)
This is an observational, cohort-based, single-site, prospective study conducted in accordance with ISO 14155-1:2003 and ISO 14155-1:2011.
- Conditions
- Body Temperature, Oxygen Saturation, Respiration, ECG
- Trial name
- NCT03206528
- Testing
- Vital Signs Monitoring System
- Where
- Israel
- Volunteers
- 100 people
- Sponsor
- G Medical Innovations Ltd.
Vital Signs
Detection of Deterioration by SNAP40 Versus Standard Monitoring in the ED
In recent years there has been increasing focus on the earlier detection of deterioration in the clinical condition of hospital patients with the aim of instigating earlier treatment to reverse this deterioration and prevent…
- Trial name
- SNAP40ED (NCT03179267)
- Testing
- SNAP40
- Where
- United Kingdom
- Volunteers
- 250 people
- Sponsor
- NHS Lothian
Vital Sign Monitoring, Vital Signs
Pulse Oximetry Performance Test for PaMo - Controlled Desaturation Test
The purpose of this study is to gather measurement data for the development and testing of a wearable patient monitor's pulse oximeter.
- Trial name
- NCT07676227
- Testing
- Hypoxia, intermittent
- Where
- Finland
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- Tampere University
Surgical Complication, Pulmonary Disease
Continuous Wireless Monitoring of Vital Signs and Automated Alerts in Participants at Home and During Hospitalization
The primary aim of this study is to test and assess the implementation and effectiveness of continuous wireless vital signs monitoring with real-time alerts on: The frequency of patients monitored with adequate data quality as…
- Conditions
- Surgical Complication, Pulmonary Disease, Hematologic Diseases, Oncology
- Trial name
- NCT05378139
- Testing
- Vital signs measurements with new app
- Where
- Denmark
- Volunteers
- 3,095 people
- Sponsor
- University Hospital Bispebjerg and Frederiksberg
Wireless Vital Signs Monitoring System, Acutely Ill Complex and Poly-pathological Patients
Role of Wireless Monitoring in Internal Medicine Unit for Ongoing Assessment of Acute Instable Patients
The present study was planned to provide clinical data on the impact of acute and critically ill patients in Internal Medicine Unit activity and economic data enabling to quantify the relative cost of acute patients management…
- Conditions
- Wireless Vital Signs Monitoring System, Acutely Ill Complex and Poly-pathological Patients, Internal Medicine Unit Mission
- Trial name
- LiMS (NCT03050034)
- Testing
- WIN @ Hospital system, Traditional monitoring
- Where
- Italy
- Volunteers
- 296 people
- Sponsor
- Azienda Socio Sanitaria Territoriale del Garda
Vital Signs
Validation of Continuous Monitoring of Vital Signs in Children With a Connected Patch
Small connected devices monitoring vital signs do not exist in children although they could be very useful to monitor patients once they have left the pediatric intensive care unit (PICU) in order to early identify patients at…
- Trial name
- VITALPICU (NCT04627766)
- Testing
- Monitoring with VT-Patch (Connected device manufactured by VitalTracer)
- Where
- Canada
- Volunteers
- 48 people
- Sponsor
- St. Justine's Hospital
Sleep
Implementation of Digital Vital Sign Monitoring to Decrease Sleep Interruption and Enhance Recovery in Phase II of the PROmoting Sleep, Patient Engagement and Recovery (PROSPER) Project
This phase II/III trial examines how a sleep enhancement intervention, including the use of wearable digital vital sign monitoring device (ViSi), affects the quality of life of cancer patients receiving acute care.
- Trial name
- NCT05456360
- Testing
- ViSi Mobile device, Sleep enhancement intervention
- Where
- United States
- Volunteers
- 89 people
- Sponsor
- M.D. Anderson Cancer Center
Critically Ill, Hemodynamic Instability
Comparing the PiCCO Monitor to the Non-invasive Biobeat (BB)-316PW in ICU Patients
The aim of this study is to compare hemodynamic monitoring using the invasive PiCCO device to the BB-613PW wireless, non-invasive PPG-based device, in critically ill patients within the ICU, suffering from hemodynamic instability…
- Trial name
- NCT04215627
- Testing
- non-invasive monitoring
- Where
- Israel
- Volunteers
- 9 people
- Sponsor
- Biobeat Technologies Ltd.
Automated Measurement of Vital Signs
Vital Signs Patch: Automated Monitoring of Vital Signs Measurements in the In-Patient Hospital Setting
This feasibility study evaluates the use of the Vital Signs Patch (VSP) System to take and monitor specified vital signs. It will be used in parallel with the normal equipment the study site uses to take and monitor vital signs.
- Trial name
- VSP (NCT02518100)
- Testing
- Vital Signs Patch (VSP) System 3-Lead (NEHB) Configuration, Vital Signs Patch (VSP) System 1-Lead (PAL) Configuration
- Where
- United States
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- LifeWatch Services, Inc.
Abdominal Cancer, Postoperative Complications
Wireless Assessment of Respiratory and Circulatory Distress; A Pilot Study
Postoperative observation of patients is based on the Early Warning Score (EWS). By using continuous wireless monitoring of vital parameters it may be possible to predict the risk of complications after abdominal cancer surgery.
- Conditions
- Abdominal Cancer, Postoperative Complications, Respiratory Complication, Circulatory; Complications
- Trial name
- WARD (NCT03102619)
- Where
- 2 sites in Denmark
- Volunteers
- 50 people
- Sponsor
- Bispebjerg Hospital
Surgical Procedure, Unspecified
VRES Study in Two Phases to Monitor Cardiac Surgical Patients Following Discharge From ICU
Failure to recognise deterioration early is a major cause of preventable deaths amongst hospital patients. The investigators wish to study whether continuous monitoring of 'vital signs' (pulse rate, breathing rate, and blood…
- Trial name
- VRES (NCT02427828)
- Testing
- Visensia Respiration Rate Estimation Service (VRES)
- Where
- United Kingdom
- Volunteers
- 208 people
- Sponsor
- OBS Medical Ltd
Vital Signs
Vital Signs Patch Early Feasibility and Usability Study
To assess the feasibility and usability of the VSP System in the in-patient hospital setting to monitor vital signs using a patch, brain, gateway, and console.
- Trial name
- VSP (NCT02521922)
- Testing
- VSP System - NEHB Configuration, VSP System - PAL Configuration
- Where
- United States
- Volunteers
- 72 people, healthy volunteers welcome
- Sponsor
- LifeWatch Services, Inc.
Critical Illness
Feasibility and Accuracy of a Wireless Vital Sign Monitor for Observation of Adult Patients in Uganda
This feasibility study will demonstrate the safety and accuracy of the Neopenda's wireless vital signs monitor, neoGuard, on 30 adult patients in a Ugandan clinical setting.
- Trial name
- NCT04761432
- Testing
- neoGuard
- Where
- Uganda
- Volunteers
- 33 people
- Sponsor
- Neopenda, PBC