comparison of the use of contactless blood pressure monitoring with established blood pressure monitoring methods
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052990
- Lead Sponsor
- Dr. Prakash K Dubey
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1.Adult ( >18 years old) ICU patient who already has an intra-arterial blood pressure measurement in place.
2.Weight between 40kg-150kgs
3.Have been connected to ICU monitor for blood pressure measurements using both IBP and CBP
4.They/ legal representative are able and willing to provide written informed consent
1.Weight below 40 kgs and above 150 kgs
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 Dozee’s signal
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the Dozee contactless BP using the IBP as the gold standard for continuous BP monitoringTimepoint: From time of admission in the ICU to 72 hours
- Secondary Outcome Measures
Name Time Method To compare the Dozee BP to cuff based CBPTimepoint: From time of admission in the ICU to 72 hours