Evaluation of EverOn™ System in Medical / Surgical Ward

Withdrawn before enrolling

Conditions studied: Post Operative Patient, Patients Requiring PCA, Respiratory Patients, Patients in Risk of Fall

In brief

The EverOn™ system developed by EarlySense, Ltd., the sponsor of this study, is intended to assist hospitals to better address and improve recognition and response to changes in a patient's condition. The system, monitors the patient while in bed consists of a contact-free sensor that is placed under the bed mattress and identifies respiratory and heart rates, degree of patient's movement or agitation while in bed as well as patient's actual exit out of the bed. The EverOn system does not require a physical contact with the patient, eliminating the need for any direct contact electrodes, leads, cuffs or nasal cannulae.

Key facts

Study ID

NCT00640718

Run by

EarlySense Ltd.

People needed

0

Starts

2008-03-01

Expected to finish

2010-05-01

Last updated by the study team

2016-07-19

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age above 18 years.
• Patients not monitored continuously by telemetry, vital sign monitor or oximetry.
• Patients not requiring special mattresses (e.g. airflow).
• The patient or a legal guardian is ready to sign the Informed Consent.

You may not qualify if…

• Patients that at the judgment of the staff in the evaluating unit, are not able to communicate coherently and respond to nurses' questions.
• Patients monitored continuously by telemetry, vital sign monitor or oximetry.
• Patients requiring special mattresses.

Where it is running

• MetroWest Medical Center — Framingham, Massachusetts, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.