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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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16 December 2017 |
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Main ID: |
NCT03177330 |
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Date of registration:
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04/06/2017 |
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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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Safety and Efficacy of Heparin Dosing Score Protocol for Polymyxin-B Hemoperfusion
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Scientific title:
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Safety and Efficacy of Heparin Dosing Score Protocol for Anticoagulation During Polymyxin-B Hemoperfusion: a Retrospective Study |
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Date of first enrolment:
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May 15, 2017 |
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Target sample size:
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30 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03177330 |
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Study type:
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Observational |
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Study design:
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Contacts
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Name:
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Chen-Tse Lee, M.D. |
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Address:
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Telephone:
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+886-2-23123456 |
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Email:
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lctbrian314@gmail.com |
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Affiliation:
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Name:
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Chen-Tse Lee, MD |
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Address:
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Telephone:
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+886972653169 |
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Email:
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lctbrian314@gmail.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- intra-abdominal septic shock patients or documented Gram-negative bacterial septic
shock patients who received polymyxin-B hemoperfusion in National Taiwan University
Hospital during October 2013-December 2016
Exclusion Criteria:
- pregnant woman
- patients with do-not-resuscitate declaration
- uncontrolled bleeding within 24hr
Age minimum:
20 Years
Age maximum:
90 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Polymyxin B Hemoperfusion
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Septic Shock
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Primary Outcome(s)
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premature cartridge clotting rate
[Time Frame: 2 hours]
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Secondary Outcome(s)
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bleeding event rate
[Time Frame: 24 hours]
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Secondary ID(s)
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201704033RIND
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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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