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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01522846 |
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Date of registration:
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09/01/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Heparin Solution and INTEM/HEPTEM Analysis
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Scientific title:
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Influence by Heparinized Flush Solution of the Radial Artery Catheter: INTEM and HEPTEM Analysis. |
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Date of first enrolment:
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January 2012 |
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Target sample size:
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25 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01522846 |
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Study type:
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Observational |
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Study design:
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Observational Model: Case-Only, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Korea, Republic of
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients requiring continuous invasive arterial pressure monitoring during operation
for anesthetic management.
Exclusion Criteria:
- heparin hypersensitivity
- hematologic disease
- anticoagulant medication
Age minimum:
20 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Cerebral Artery Anuerysm
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Spinal Stenosis
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Brain Tumor
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Intervention(s)
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Drug: Heparin
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Primary Outcome(s)
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HEPTEM test
[Time Frame: at 30 min before operation and 30 min after operation]
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INTEM test
[Time Frame: at 30 min before operation and 30 min after operation]
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Secondary Outcome(s)
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Total infused units of heparin
[Time Frame: periond from starting operation to finishing operation (espected average of 5 hours).]
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Secondary ID(s)
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B_1112_069_003
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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