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Clinical Implication of the Tunable Crack Sensor

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ClinicalTrials.gov Identifier: NCT03805815
Recruitment Status : Active, not recruiting
First Posted : January 16, 2019
Last Update Posted : January 16, 2019
Sponsor:
Information provided by (Responsible Party):
Bon-Kwon Koo, Seoul National University Hospital

Brief Summary:
[Development of diagnosis algorism for paroxysmal arrhythmia using ultra-thin resistive membrane: a pilot study] Comparison of blood pressure via tunable crack sensor and invasive pressure wire

Condition or disease Intervention/treatment
Blood Pressure Device: tunable crack sensor

Detailed Description:
To develop a diagnosis algorism for paroxysmal arrhythmia using ultra-thin resistive membrane, we will compare the blood pressure measured via a tunable crack sensor and that measured by a invasive pressure wire

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Study Type : Observational
Actual Enrollment : 30 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Development of Diagnosis Algorism for Paroxysmal Arrhythmia Using Ultra-thin Resistive Membrane: a Pilot Study
Actual Study Start Date : September 10, 2018
Estimated Primary Completion Date : March 1, 2019
Estimated Study Completion Date : August 1, 2019

Intervention Details:
  • Device: tunable crack sensor
    blood pressure monitoring via crack sensor


Primary Outcome Measures :
  1. Blood pressure monitoring using tunable crack sensor [ Time Frame: immediately ]
    Systolic blood pressure and diastolic blood pressure by using tunable crack sensor



Information from the National Library of Medicine

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Ages Eligible for Study:   19 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
A case of suspected coronary artery disease for the purpose of coronary angiography
Criteria

Inclusion Criteria:

A case of suspected coronary artery disease at Seoul National University Hospital for the purpose of coronary angiography

  • At least 19 years old
  • If he/she hears enough explanation about clinical research and intends to participate in clinical research himself

Exclusion Criteria:

  • Under 19 years old
  • Refusal to participate in clinical studies
  • If the cognitive function is weak enough not to understand the explanation of the clinical study and to make voluntary decisions accordingly

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03805815


Locations
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Korea, Republic of
Seoul national university hospital
Seoul, Korea, Republic of, 110-744
Sponsors and Collaborators
Seoul National University Hospital
Investigators
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Principal Investigator: Bon-Kwon Koo Seoul National University Hospital

Publications:
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Responsible Party: Bon-Kwon Koo, Professor of Medicine / Cardiology, Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT03805815     History of Changes
Other Study ID Numbers: H-1808-177-969
First Posted: January 16, 2019    Key Record Dates
Last Update Posted: January 16, 2019
Last Verified: January 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Bon-Kwon Koo, Seoul National University Hospital:
blood pressure
crack sensor