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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00875602
Other study ID # CHW ES-MRK-PROT-6
Secondary ID
Status Withdrawn
Phase N/A
First received April 2, 2009
Last updated December 5, 2016
Start date April 2009

Study information

Verified date October 2012
Source EarlySense Ltd.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Evaluation of continuous monitoring device on patients Risk during hospitalization and nurse satisfaction level.


Description:

To assess the effects of continuous patient monitoring using a contactless monitor in a medical-surgical unit on transfers and length of stay at higher level of care units


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Hospitalized patients

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Post Surgical Pat., Medical Pat., Resp. Failure, Car.Arrest, Death

Intervention

Device:
EverOn (EarlySense) contactless monitoring device
Hospitalized patients on the study unit are monitored by a contactless device

Locations

Country Name City State
United States CHMC Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
EarlySense Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evidence of benefit to caregivers and patients 12 month No