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Eval EarlySense Bet Lowenstein Sleeplab

NCT01978340 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2016-07-19

No results posted yet for this study

Summary

The study objective is to collect heart rate, respiration rate and motion data of patients admitted to sleep lab and to determine the accuracy level of the EarlySense system vs. the monitors used in sleep lab (e.g., Polysomnography, respiratory belts, ECG, etc..) . Data regarding sleep condition, scoring and quality of sleep and in and out of bed status, patient turns will also be collected and compared to data collected by EarlySense contactless monitor. Different patient population will be monitored including obese, morbidly obese, patients with or without obstructive/central apnea, patients with or without arrhythmia as well as healthy population who arrive to sleep lab for general evaluation will be monitored

Conditions

  • Obese
  • Sleep Apnea, Obstructive
  • Central Apnea
  • Sleep Disorders
  • Poor Quality Sleep

Sponsors & Collaborators

  • EarlySense Ltd.

    lead INDUSTRY

Principal Investigators

  • Tatiana Vander, MD · Beit Lowenstein Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2014-02-28
Completion
2014-04-30

Countries

  • Israel

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01978340 on ClinicalTrials.gov