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Safety and Efficacy of Heparin Dosing Score Protocol for Polymyxin-B Hemoperfusion

Safety and Efficacy of Heparin Dosing Score Protocol for Anticoagulation During Polymyxin-B Hemoperfusion: a Retrospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03177330
Enrollment
30
Registered
2017-06-06
Start date
2017-05-15
Completion date
2017-07-31
Last updated
2017-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polymyxin B Hemoperfusion, Septic Shock

Brief summary

Polymyxin B hemoperfusion (PMX-HP) is mainly used to remove endotoxins in septic shock patients with intra-abdominal infections. Because of the concerns of postoperative bleeding, physicians may hesitate to use anticoagulation in patients with septic shock within a few hours after an abdominal operation. We developed a heparin dosing score protocol for heparin dosage adjustment. The purpose of the study is to examine the safety and efficacy of the heparin dosing score protocol.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
premature cartridge clotting rate2 hoursthe incidence of premature cartridge clotting within 2hr

Secondary

MeasureTime frameDescription
bleeding event rate24 hoursthe incidence of substantial bleeding event within 24hr

Countries

Taiwan

Contacts

Primary ContactChen-Tse Lee, MD
lctbrian314@gmail.com+886972653169

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026