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Evaluation of EverOn™ - A Contact-Free System for Measuring Heart Rate, Respiratory Rate and Motion

E

EarlySense

Status

Withdrawn

Conditions

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

Treatments

Device: EverOn (EarlySense) contactless monitoring device

Study type

Interventional

Funder types

Industry

Identifiers

NCT00875602
CHW ES-MRK-PROT-6

Details and patient eligibility

About

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

Full 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

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized patients

Exclusion criteria

  • None

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

control
No Intervention group
Description:
before-after (retrospective) and concurrent controls as comparators with a prospective intervention group
Study unit
Active Comparator group
Description:
Hospitalized patients in the study group will be continously monitored / supervised by the contact-free device
Treatment:
Device: EverOn (EarlySense) contactless monitoring device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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