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Therapeutic Plasmaexchange in Early Septic Shock (EXCHANGE)

Primary Purpose

Septic Shock

Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
TPE
Sponsored by
Hannover Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring Septic shock, Therapeutic plasma exchange, Sepsis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hannover Medical School
  • University Hospital Bonn

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

TPE

SMT

Arm Description

additive singular therapeutic plasma Exchange (TPE) using fresh frozen Plasma (FFP) as replacement fluid

Standard medical Treatment (SMT) for septic shock following the present surviving sepsis guidelines

Outcomes

Primary Outcome Measures

Norepinephrine dose
Vasopressor dose reduction as indicator of shock reversal

Secondary Outcome Measures

Mean Sequential organ failure assessment (SOFA) score
SOFA score as indicator of organ dysfunction
percent change of ADAMTS-13 activity from baseline
(will only be analyzed in the Hannover cohort)
percent change of activated Protein C activity from baseline
(will only be analyzed in the Hannover cohort)
percent change of permeability factors angiopoietin-1, -2 and sTie-2 from baseline
permeability and anti-permeability factors (will only be analyzed in the Hannover cohort)
28 day survival

Full Information

First Posted
January 13, 2020
Last Updated
February 6, 2021
Sponsor
Hannover Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT04231994
Brief Title
Therapeutic Plasmaexchange in Early Septic Shock
Acronym
EXCHANGE
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
July 31, 2020 (Actual)
Study Completion Date
August 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hannover Medical School

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
Septic shock, Therapeutic plasma exchange, Sepsis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TPE
Arm Type
Experimental
Arm Description
additive singular therapeutic plasma Exchange (TPE) using fresh frozen Plasma (FFP) as replacement fluid
Arm Title
SMT
Arm Type
No Intervention
Arm Description
Standard medical Treatment (SMT) for septic shock following the present surviving sepsis guidelines
Intervention Type
Device
Intervention Name(s)
TPE
Intervention Description
singular Therapeutic Plasma Exchange using fresh frozen Plasma as replacement fluid
Primary Outcome Measure Information:
Title
Norepinephrine dose
Description
Vasopressor dose reduction as indicator of shock reversal
Time Frame
6 hours after randomization
Secondary Outcome Measure Information:
Title
Mean Sequential organ failure assessment (SOFA) score
Description
SOFA score as indicator of organ dysfunction
Time Frame
day 1-8 following randomization
Title
percent change of ADAMTS-13 activity from baseline
Description
(will only be analyzed in the Hannover cohort)
Time Frame
6 hours after randomization
Title
percent change of activated Protein C activity from baseline
Description
(will only be analyzed in the Hannover cohort)
Time Frame
6 hours after randomization
Title
percent change of permeability factors angiopoietin-1, -2 and sTie-2 from baseline
Description
permeability and anti-permeability factors (will only be analyzed in the Hannover cohort)
Time Frame
6 hours after randomization
Title
28 day survival
Time Frame
after 28 days following randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sascha David, MD
Organizational Affiliation
Clinic for nephrology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Klaus Stahl, MD
Organizational Affiliation
Clinic for gastroenterology and hepatology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hannover Medical School
City
Hannover
State/Province
Lower Saxony
ZIP/Postal Code
30625
Country
Germany
Facility Name
University Hospital Bonn
City
Bonn
ZIP/Postal Code
53127
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
pre-defined substudies
Citations:
PubMed Identifier
33471132
Citation
David S, Bode C, Putensen C, Welte T, Stahl K; EXCHANGE study group. Adjuvant therapeutic plasma exchange in septic shock. Intensive Care Med. 2021 Mar;47(3):352-354. doi: 10.1007/s00134-020-06339-1. Epub 2021 Jan 20. No abstract available.
Results Reference
result
PubMed Identifier
35551628
Citation
Stahl K, Wand P, Seeliger B, Wendel-Garcia PD, Schmidt JJ, Schmidt BMW, Sauer A, Lehmann F, Budde U, Busch M, Wiesner O, Welte T, Haller H, Wedemeyer H, Putensen C, Hoeper MM, Bode C, David S. Clinical and biochemical endpoints and predictors of response to plasma exchange in septic shock: results from a randomized controlled trial. Crit Care. 2022 May 12;26(1):134. doi: 10.1186/s13054-022-04003-2.
Results Reference
derived
PubMed Identifier
34817751
Citation
Stahl K, Hillebrand UC, Kiyan Y, Seeliger B, Schmidt JJ, Schenk H, Pape T, Schmidt BMW, Welte T, Hoeper MM, Sauer A, Wygrecka M, Bode C, Wedemeyer H, Haller H, David S. Effects of therapeutic plasma exchange on the endothelial glycocalyx in septic shock. Intensive Care Med Exp. 2021 Nov 24;9(1):57. doi: 10.1186/s40635-021-00417-4.
Results Reference
derived
Links:
URL
https://pubmed.ncbi.nlm.nih.gov/33471132/
Description
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