No Specific Conditions

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Review clinical trials related to No Specific Conditions. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Validating Dozee for Contactless Monitoring of Heart, Breathing, and Movemen

The Dozee VS system (K221555) is a contactless device that tracks heart rate and breathing rate using a sensor sheet placed under the mattress. It captures body vibrations and converts them into vital signs, which can be monitored remotely in real time. The system also supports add-ons like a blood pressure cuff, pulse oximeter, and thermometer, offering a complete monitoring solution. This study aims to validate the updated AI-powered heart rate and improved breathing rate algorithms across different sensor sheet types to confirm clinical accuracy

Participants needed: 60
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: Turtle Shell Technologies Pvt. Ltd.Updated: Nov 3, 2025Locations: 1
Eligibility criteria

Adults Male or female. (Above 18 years of age) [+4]

Are connected to a device that may interfere with the device monitoring in this... [+4]

Status: Not yet recruiting

Machine Learning and 3D Image-based Modeling for Body Weight Estimation.

The goal of this randomized controlled clinical trial is to \[learn about, test, compare etc.\] in critically ill or injured cohorts of patients presenting to the Emergency Department. The main question\[s\] it aims to answer are: * Are weight estimates from a 3D camera system more accurate than standard methods of weight estimation? * Do patients who receive weight estimates with a 3D camera system have fewer drug dosing errors than patients receiving standard care? Participants will either receive a weight estimate using a 3D camera system, or standard methods of care. Researchers will compare the 3D camera group to those with standard care to see if the weight estimates are more accurate, to see if drug dosing is more accurate, and to compare the incidence of adverse events related to medications in each group.

Participants needed: 320
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Florida Atlantic UniversityUpdated: Jun 6, 2025
Eligibility criteria

Patients who are unable to provide consent. [+1]