- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03201289
Microvolt T-wave Alternans in Cardiac Surgery Patients
June 27, 2017 updated by: Yunseok Jeon, Seoul National University Hospital
The purpose of this study is to measure MTWA in the patients undergoing cardiac surgery and to investigate the relation between MTWA and adverse clinical outcomes.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
224
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Seoul, Korea, Republic of, 03080
- Seoul National University Hospital
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients undergoing cardiac surgery
Description
Inclusion Criteria:
- All patients underwent cardiac surgery including coronary artery bypass graft surgery with or without cardiopulmonary bypass, cardiac valve surgery, cardiac mass excision, thoracic aorta surgery, etc.
Exclusion Criteria:
- unavailability of the recording equipment
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 |
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Cardiac surgery
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
in hospital mortality
Time Frame: up to 3 months(during hospital stay)
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in hospital death
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up to 3 months(during hospital stay)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
postoperative complication
Time Frame: up to 3 months(during hospital stay)
|
The secondary end points were myocardial infarction, ventricular tachycardia, atrial fibrillation, cardiogenic shock, stroke, coma, renal failure, respiratory failure, and length of stay in intensive care unit (ICU) and hospital.
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up to 3 months(during hospital stay)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
January 1, 2013
Primary Completion (Actual)
December 29, 2016
Study Completion (Actual)
December 29, 2016
Study Registration Dates
First Submitted
June 16, 2017
First Submitted That Met QC Criteria
June 27, 2017
First Posted (Actual)
June 28, 2017
Study Record Updates
Last Update Posted (Actual)
June 28, 2017
Last Update Submitted That Met QC Criteria
June 27, 2017
Last Verified
June 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MTWA
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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