PolyMyXin-B direct hemoperfusion OPTimal Initiation timing with Catecholamine study (PMX-OPTIC study)
Not Applicable
- Conditions
- Septic shock
- Registration Number
- JPRN-UMIN000051464
- Lead Sponsor
- Teikyo University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 600
Inclusion Criteria
Not provided
Exclusion Criteria
1. Cases of End of Life/Terminal Care where treatment was not the primary objective. 2. Patients who received interventions for circulatory support such as ECMO, VAD, IMPELLA (excluding IABP).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method