Evaluation of the usefulness of noninvasive monitoring device for seriously ill patients
Not Applicable
- Conditions
- critically ill patients
- Registration Number
- JPRN-UMIN000022001
- Lead Sponsor
- Chiba University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Not provided
Exclusion Criteria
(1)The patient who puts on the IABP and the PCPS. (2)The patient who is not suitable for the wearing of the device for a burn and other skin problems. (3)The patient who receives an examination of MRI during an examination. (4)The patient who receives an treatment of hyperbaric oxygen therapy during an examination (5)The patient who has hypersensitivity to infrared rays and transmitted light. (6)The patient whom it was judged not to be able to carry out an examination safely by a doctor.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome is to evaluate the equivalency between the measurements of the blood pressure(systolic, diastolic, and mean blood pressure) to be provided by a new device and the measurements of the blood pressure to be provided by an arterial pressure line.
- Secondary Outcome Measures
Name Time Method