The Pilot Study of the Efficacy of Polymyxin-B Hemoperfusion in Critically Ill Patients With Severe Sepsis
NCT02413541 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90
Last updated 2021-03-05
Summary
This research project is a study to immunology changes in critically ill patients with severe sepsis by using Endotoxin Activity Assay (EAA) combined with Polymyxin-B Hemoperfusion.
Conditions
- Severe Sepsis
Interventions
- PROCEDURE
-
Polymyxin-B Hemoperfusion
Endotoxin removal
- PROCEDURE
-
Standard treatment
Sponsors & Collaborators
-
Chulalongkorn University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-31
- Primary Completion
- 2015-12-31
- Completion
- 2017-08-30
Countries
- Thailand
Study Locations
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