Validation of contact less Blood pressure monitoring device

Not Applicable

• Conditions: Health Condition 1: X- New Technology

• Registration Number: CTRI/2022/06/043075
• Lead Sponsor: Turtle Shell Technologies

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Weight between 40 kgs to 150 kgs

2. Have been connected to ICU monitor for blood pressure measurements using both IBP and CBP

3. They/ legal representative are able and willing to provide written informed consent

Exclusion Criteria

Weight below 40kgs and above 150kgs

2. Currently pregnant

3. Have any condition that could interfere with the subjects ability to tolerate continuous monitoring with IBP or periodic monitoring with CBP

4. Exhibit injuries, deformities, intravenous lines, or other abnormalities that, in the opinion of the investigator, may prevent proper cuff application or functioning

5. Level of agitation or non-compliance too high to enroll in opinion of PI

6. Needs the use of equipments whose operation can interfere with Dozeeâ??s signal

7. A significant medical condition in the judgment of the investigator, which

may compromise the study testing procedures

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sensitivity and Accuracy of Dozee in matching the BP values from IBP and CBPTimepoint: Continuous monitoring up to 72 hours

Secondary Outcome Measures

Name	Time	Method
ATimepoint: NA