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Pressure Sensitive Mats for Patient Monitoring in the NICU

NCT03224286 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2021-06-24

No results posted yet for this study

Summary

This is a pilot study that provides the investigators with an opportunity to assess the application of PSM technology for patient monitoring in the NICU. This is a prospective, observational, cohort study.The investigators expect the duration of infant participation in this study to be 6 hours per single recording session with no follow-up required.

Conditions

  • Apnea
  • Respiration Disorder

Interventions

DEVICE

Pressure sensitive mat

Infant placed on pressure sensitive mat and has physiological parameters recorded.

Sponsors & Collaborators

  • NSERC Collaborative Research and Development

    collaborator UNKNOWN

  • Children's Hospital of Eastern Ontario

    lead OTHER

Principal Investigators

  • JoAnn Harrold, MD · Children's Hospital of Eastern Ontario

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-22
Primary Completion
2020-06-15
Completion
2020-06-15

Countries

  • Canada

Study Locations

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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 NCT03224286 on ClinicalTrials.gov