- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03827369
The Blood Pressure Analysis on Critically Ill Patients
March 26, 2020 updated by: Taoyuan General Hospital
The study is to explore the relationship between coefficient of variation of harmonic magnitude (HCV) and different organ failures among those critically ill patients.
In the future, we can act as a warning system on patients with multiple organ failures or terminal illness, also as an indicator of treatment effect.
Study Overview
Status
Unknown
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tzu-Yi Chuang
- Phone Number: 3787 886-3-3699721
- Email: revival_chuang@yahoo.com
Study Locations
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Taoyuan, Taiwan, 33004
- Recruiting
- Taoyuan General Hospital, Ministry of Health and Welfare
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients without severe arrhythmia admitted to the ICU of Taoyuan General Hospital.
Description
Inclusion Criteria:
- ICU patients in the 20-to-99 age range
- Subjects agree to sign the Informed Consent Form and are willing to cooperate with Arterial pulse measurement
Exclusion Criteria:
- Subject has severe arrhythmia
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
ICU patient
Pulse pressure of the radical artery was obtained by arterial line.
The output of the transducer was connected to an IBM PC for analysis via an A/D converter with sampling rate = 250 datapoints/sec.
The pulse spectrum was analyzed with the Fourier transformation using T (period) = 1 pulse time.
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Our study is to measure the coefficient of variation of the HCV of the radial arterial pulse among ICU patients with multiple organ failures (MOF).
Patients admitted to Taoyuan General Hospital were recorded during the 6 months study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Coefficient of variation of harmonic magnitude
Time Frame: 15 min
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We measure the blood pressure of participants with multiple organ failures (MOF) by pressure transducer during the 6 months study in the ICU of Taoyuan General Hospital.
The radial artery pressure pulse of both hands are recorded with a pressure transducer fixed on the skin with tape and an adjustable belt with a small button to achieve suitable pressure.
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15 min
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tzu-Yi Chuang, Taoyuan General Hospital, Minstry of Healthy and Welfare
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 30, 2019
Primary Completion (Anticipated)
December 1, 2020
Study Completion (Anticipated)
December 1, 2020
Study Registration Dates
First Submitted
January 30, 2019
First Submitted That Met QC Criteria
January 31, 2019
First Posted (Actual)
February 1, 2019
Study Record Updates
Last Update Posted (Actual)
March 27, 2020
Last Update Submitted That Met QC Criteria
March 26, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TYGH107041
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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