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Therapeutic Plasmaexchange in Early Septic Shock

Prospective, Randomized, Single-center, Open-label, Parallel-group Trial Investigating the Efficacy of Therapeutic Plasma Exchange as an Adjunctive Strategy Against Early Septic Shock - Effect on Hemodynamics and Biochemical Markers

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04231994
Acronym
EXCHANGE
Enrollment
40
Registered
2020-01-18
Start date
2018-06-01
Completion date
2020-08-31
Last updated
2021-02-10

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

Conditions

Septic Shock

Keywords

Septic shock, Therapeutic plasma exchange, Sepsis

Brief summary

Sepsis is defined by the occurrence of critical organ dysfunction in the context of infection. Unfortunately, its incidence appears to be rising, and the mortality of septic shock remains extraordinary high (\> 60%). Death in sepsis arises from shock and multi organ dysfunction that are - at least in part - triggered by an inadequate response of the host's immune system to the infection. Given the injurious role of 1) this overwhelming immune response and 2) the consumption of protective plasmatic factors (e.g. vWF cleaving proteases, hemostatic factors etc.) while the disease is progressing the investigators hypothesize that early therapeutic plasma exchange (TPE) in the most severely ill individuals might improve hemodynamics, oxygenation and ultimately survival. This therapeutic strategy combines 2 major aspects in 1 procedure: 1. removal of harmful circulating molecules and 2. replacement of protective plasma proteins. The investigators designed the EXCHANGE trial to analyze in a randomized fashion the benefit of TPE as an add-on treatment to state of the art standard sepsis care. Only patients with early septic shock (\< 24 hrs) and high catecholamine doses (norepinephrine \> 0.4 ug/kg body weight/min) will be included. Those in the treatment group will receive 1 TPE within 2 hours following randomization. The primary outcome is norepinephrine dose 6 hrs after randomization. The recruitment period is 2 years and will be performed at the Hannover medical School University hospital in Germany. Secondary endpoints (including organ dysfunction as well as biochemical markers of inflammation and coagulation) will be assessed on day 1-8 and day 28 after TPE. The investigators hope to demonstrate a potential benefit of an additive treatment approach to improve the outcome of patients suffering from septic shock.

Interventions

DEVICETPE

singular Therapeutic Plasma Exchange using fresh frozen Plasma as replacement fluid

Sponsors

Hannover Medical School
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Onset of septic shock within less than 24 hrs * Norepinephrine dose of ≥ 0.4 ug/kg/min bodyweight (target mean arterial pressure ≥ 65 mmHg) ≥ 30 min

Exclusion criteria

* Age\<18 years and \> 80 years * Pregnancy * Known history of transfusion reactions

Design outcomes

Primary

MeasureTime frameDescription
Norepinephrine dose6 hours after randomizationVasopressor dose reduction as indicator of shock reversal

Secondary

MeasureTime frameDescription
Mean Sequential organ failure assessment (SOFA) scoreday 1-8 following randomizationSOFA score as indicator of organ dysfunction
percent change of ADAMTS-13 activity from baseline6 hours after randomization(will only be analyzed in the Hannover cohort)
percent change of activated Protein C activity from baseline6 hours after randomization(will only be analyzed in the Hannover cohort)
percent change of permeability factors angiopoietin-1, -2 and sTie-2 from baseline6 hours after randomizationpermeability and anti-permeability factors (will only be analyzed in the Hannover cohort)
28 day survivalafter 28 days following randomization

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026