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Clinical Trials/NCT03240926
NCT03240926
Completed
Not Applicable

Loop Band Validation Study

Spry Health1 site in 1 country235 target enrollmentFebruary 21, 2017
ConditionsCOPD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD
Sponsor
Spry Health
Enrollment
235
Locations
1
Primary Endpoint
Device Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate) measured by Arterial Line.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The main purpose of this study is to assess the accuracy of a non-invasive wearable technology in the form of a wristband.

Detailed Description

The main purpose of this study is to assess the accuracy of a non-invasive wearable technology in the form of a wristband. This wristband (Loop Band) uses optical sensors and spectrometry to measure and estimate vitals as well as a full blood gas panel; comparable to the standard method of an invasive arterial line and pressure transducer. The investigators aim to show equivalence of clinical physiologic outcome measurements with the Loop Band relative to current methods (i.e. arterial lines, etc.). In addition, this study aims to validate this wearable technology as a potential alternative to invasive measurements, to reduce complications, and improve accuracy in regards to patient monitoring.

Registry
clinicaltrials.gov
Start Date
February 21, 2017
End Date
January 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Spry Health
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient has capacity to consent for the study.
  • Anesthetic plan for an arterial line for vital sign monitoring during their surgical procedure.

Exclusion Criteria

  • Active Atrial Fibrillation
  • Active C-difficile
  • Amputation of the arm at the wrist or above
  • The Investigator and/or Clinical Research Nurse will conduct a visual inspection for attributes that may diminish device accuracy. These include but are not limited to: tattoos over the radial artery, burns or heavy scarring over the radial artery, fragile skin, any skin diseases affecting the wrist or arm, Physician discretion-any condition deemed inappropriate that will preclude use of the device.

Outcomes

Primary Outcomes

Device Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate) measured by Arterial Line.

Time Frame: intraoperative

Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate etc.) with the Loop Band relative to current methods (i.e. arterial lines, etc.) during a surgical procedure.

Secondary Outcomes

  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability](intraoperative)

Study Sites (1)

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