Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02570906
Other study ID # COVMOPO0517
Secondary ID
Status Completed
Phase N/A
First received September 1, 2015
Last updated February 25, 2016
Start date December 2015
Est. completion date February 2016

Study information

Verified date February 2016
Source Medtronic - MITG
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study will evaluate the performance of the Zephyr BioPatch in measuring heart rate, respiration rate, posture, and activity level compared to reference devices in healthy adult subjects during a variety of situations including hospital room movements, talking, and a short bout of exercise.


Other known NCT identifiers
  • NCT02606968

Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date February 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Signed and dated informed consent by subject or legally authorized representative (LAR)

2. Male or female of any race

3. 18-50 years of age, inclusive

4. Willingness to have study devices attached during study participation

5. Willingness to participate in all aspects of the study

6. Ability to walk without human assistance or walking aides (e.g. cane or walker), in the opinion of the investigator

Exclusion Criteria:

1. Subject is unable to provide informed consent

2. Under 18 years of age or over 50 years of age

3. Implanted pacemaker or defibrillator

4. Diagnosis of atrial fibrillation as reported by the subject

5. Current hospital admission

6. History of hospital admission or a surgical procedure in the 60 days prior to study enrollment

7. Any contraindications to protocol specific repositioning techniques (e.g. turning on right side or left side or lying in supine position)

8. Female subject is pregnant and/or lactating as reported by the subject

9. Subject is considered as being morbidly obese (defined as BMI >39.5)

10. Subject is on any medications, in the opinion of the investigator, that would impair heart response during the short bout of exercise

11. A serious concurrent medical or other condition, in the opinion of the investigator, that would impair protocol compliance or safety of the subject

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Zephyr BioPatch
Remote patient monitoring devices: BioPatchâ„¢ (ZephyrLIFE Hospital Systemâ„¢)

Locations

Country Name City State
United States Columbia University Medical Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Medtronic - MITG

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart rate accuracy No follow-up visits will occur On the day of enrollment to completion of one-time study visit No
Primary Heart rate precision No follow-up visits will occur On the day of enrollment to completion of one-time study visit No
Primary Respiratory rate accuracy No follow-up visits will occur On the day of enrollment to completion of one-time study visit No
Primary Respiratory rate precision No follow-up visits will occur On the day of enrollment to completion of one-time study visit No
Primary Activity Activity will be classified as lying, upright, walking, or running. On the day of enrollment to completion of one-time study visit No
Primary Body orientation (position) Body orientation (position) if lying horizontally will be classified as facing right, facing left, facing down (prone), or facing up (supine). On the day of enrollment to completion of one-time study visit No
See also
  Status Clinical Trial Phase
Withdrawn NCT02970903 - VitalPAD: an Intelligent Monitoring and Communication Device to Optimize Safety in the PICU N/A
Withdrawn NCT01612091 - The Monitoring Messenger: Mobile Patient Monitoring for the Pediatric Intensive Care Unit N/A
Completed NCT02041858 - Effect of Altered Alarm Settings on Patient Adverse Events and Alarm Signal Frequency N/A