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Effects of Hemoperfusion With a Polymyxin B Membrane in Peritonitis With Septic Shock (ABDO-MIX)

Primary Purpose

Peritonitis, Septic Shock

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
standard therapy
hemoperfusion
Sponsored by
Meditor SAS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peritonitis focused on measuring peritonitis, septic shock, hemoperfusion, Polymyxin B, endotoxin

Eligibility Criteria

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

Inclusion Criteria:

  • Confirmed community or nosocomial acquired peritonitis due to organ perforation
  • Septic shock requiring catecholamine infusion started or maintained 2 hours after surgery

Exclusion Criteria:

  • Pregnancy
  • No severity criteria within the 8 hours following surgery
  • Neutropenia due to chemotherapy or malignancy
  • Abdominal sepsis without peritonitis
  • Mesenteric ischemia without perforation
  • Peritonitis due to appendicitis
  • Perforation linked to trauma
  • Cirrhosis child C
  • Impossibility to use heparin
  • Prolonged cardiac arrest within 72h before surgery
  • Terminal disease diagnosed during surgery
  • Moribund subjects

Sites / Locations

  • Clermont-Ferrand University Hospital
  • Dieppe Hospital
  • Vendée Hospital
  • Dr Schaffner Hospital
  • Lille University Hospital
  • Limoges University Hospital
  • La Source Hospital
  • Lariboisière University Hospital
  • Saint Louis Hospital
  • Saint Jean Hospital
  • Bordeaux University Hospital
  • Poitiers University Hospital
  • Pontchaillou University Hospital
  • Roanne Hospital
  • Rouen University Hospital
  • Saint-Malo Hospital
  • Strasbourg University Hospital
  • Tours University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Standard therapy

Hemoperfusion

Arm Description

Standard therapy in the ICU including but not limited to: antibiotic therapy, nutrition, fluid challenge, vasopressors, hemodynamic monitoring, organ support in the ICU including mechanical ventilation, renal replacement therapy when appropriate

standard therapy + 2 sessions of hemoperfusion within the first 24 hours

Outcomes

Primary Outcome Measures

Mortality

Secondary Outcome Measures

organ failure assessed by SOFA score
delay to withdraw catecholamine after initial shock
mortality between the two groups at 7 dayx, 14 days, 21 days and 90 days
number of participants with adverse events related to hemoperfusion technique including anticoagulation therapy such as bleeding (type and number of blood transfusion)

Full Information

First Posted
October 8, 2010
Last Updated
December 17, 2013
Sponsor
Meditor SAS
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1. Study Identification

Unique Protocol Identification Number
NCT01222663
Brief Title
Effects of Hemoperfusion With a Polymyxin B Membrane in Peritonitis With Septic Shock
Acronym
ABDO-MIX
Official Title
Effects of Hemoperfusion With a Polymyxin B Membrane in Peritonitis With Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Meditor SAS

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this randomized, comparative, open and multi-centre study is to show that two sessions of hemoperfusion with Toraymyxin performed within maximum 36 hours after the surgery of a peritonitis by hollow organ perforation reduce the mortality in patients suffering from septic shock.
Detailed Description
The mortality rate due to peritonitis associated to a severe sepsis or a septic shock remains high (between 40 and 60% as per the studies). The recent complementary therapies for severe sepsis have been reassessed (strict glycaemic control, substitutive corticotherapy, activated protein C). Early neutralisation of the endotoxaemia related to gram-negative bacilli sepsis in contact with hemoperfusion membrane covered with polymyxin B (Toraymyxin™) may enable reduction of the inflammatory reaction caused by sepsis and improve its prognosis. 30 studies, including 10 randomized studies, have compared hemoperfusion with Toraymyxin™ to the standard treatment, showing an improvement in the patients' haemodynamic state, oxygenation conditions and reduction in mortality. This treatment is commonly used in Japan. However, the studies conducted either include only a limited number of patients or are not randomized prospective studies. The post-hoc analysis of a recent randomized study conducted on a limited number of patients with abdominal septic shock shows a significant reduction in mortality after factor adjustment. Though the side effects of such a treatment are limited, its cost is high. Hence, extensive prospective studies are necessary to confirm its effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peritonitis, Septic Shock
Keywords
peritonitis, septic shock, hemoperfusion, Polymyxin B, endotoxin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
243 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard therapy
Arm Type
Other
Arm Description
Standard therapy in the ICU including but not limited to: antibiotic therapy, nutrition, fluid challenge, vasopressors, hemodynamic monitoring, organ support in the ICU including mechanical ventilation, renal replacement therapy when appropriate
Arm Title
Hemoperfusion
Arm Type
Experimental
Arm Description
standard therapy + 2 sessions of hemoperfusion within the first 24 hours
Intervention Type
Device
Intervention Name(s)
standard therapy
Intervention Description
Standard therapy in the ICU including but not limited to: antibiotic therapy, nutrition, fluid challenge, vasopressors, hemodynamic monitoring, organ support in the ICU including mechanical ventilation, renal replacement therapy when appropriate
Intervention Type
Device
Intervention Name(s)
hemoperfusion
Other Intervention Name(s)
toraymyxin, PMX-20R
Intervention Description
Extracorporeal hemoperfusion with Toraymyxin PMX-20R and conventional medical therapy in the ICU including but not limited to: antibiotic therapy, nutrition, fluid challenge, vasopressors, hemodynamic monitoring, organ support in the ICU including mechanical ventilation, renal replacement therapy when appropriate.
Primary Outcome Measure Information:
Title
Mortality
Time Frame
28 days
Secondary Outcome Measure Information:
Title
organ failure assessed by SOFA score
Time Frame
day 3
Title
delay to withdraw catecholamine after initial shock
Time Frame
day 1-day 28
Title
mortality between the two groups at 7 dayx, 14 days, 21 days and 90 days
Time Frame
90 days
Title
number of participants with adverse events related to hemoperfusion technique including anticoagulation therapy such as bleeding (type and number of blood transfusion)
Time Frame
day1-day4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed community or nosocomial acquired peritonitis due to organ perforation Septic shock requiring catecholamine infusion started or maintained 2 hours after surgery Exclusion Criteria: Pregnancy No severity criteria within the 8 hours following surgery Neutropenia due to chemotherapy or malignancy Abdominal sepsis without peritonitis Mesenteric ischemia without perforation Peritonitis due to appendicitis Perforation linked to trauma Cirrhosis child C Impossibility to use heparin Prolonged cardiac arrest within 72h before surgery Terminal disease diagnosed during surgery Moribund subjects
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Didier Payen, MD
Organizational Affiliation
Lariboisière University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
René Robert, MD
Organizational Affiliation
Poitiers University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clermont-Ferrand University Hospital
City
Clermont-Ferrand
ZIP/Postal Code
63058
Country
France
Facility Name
Dieppe Hospital
City
Dieppe
ZIP/Postal Code
76202
Country
France
Facility Name
Vendée Hospital
City
La Roche sur Yon
ZIP/Postal Code
85925
Country
France
Facility Name
Dr Schaffner Hospital
City
Lens
ZIP/Postal Code
62307
Country
France
Facility Name
Lille University Hospital
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Limoges University Hospital
City
Limoges
ZIP/Postal Code
87042
Country
France
Facility Name
La Source Hospital
City
Orleans
ZIP/Postal Code
45067
Country
France
Facility Name
Lariboisière University Hospital
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Saint Louis Hospital
City
Paris
ZIP/Postal Code
75475
Country
France
Facility Name
Saint Jean Hospital
City
Perpignan
ZIP/Postal Code
66046
Country
France
Facility Name
Bordeaux University Hospital
City
Pessac
ZIP/Postal Code
33600
Country
France
Facility Name
Poitiers University Hospital
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Pontchaillou University Hospital
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
Roanne Hospital
City
Roanne
ZIP/Postal Code
42300
Country
France
Facility Name
Rouen University Hospital
City
Rouen
ZIP/Postal Code
76031
Country
France
Facility Name
Saint-Malo Hospital
City
Saint-Malo
ZIP/Postal Code
35403
Country
France
Facility Name
Strasbourg University Hospital
City
Strasbourg
ZIP/Postal Code
67091
Country
France
Facility Name
Tours University Hospital
City
Tours
ZIP/Postal Code
37044
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
25862039
Citation
Payen DM, Guilhot J, Launey Y, Lukaszewicz AC, Kaaki M, Veber B, Pottecher J, Joannes-Boyau O, Martin-Lefevre L, Jabaudon M, Mimoz O, Coudroy R, Ferrandiere M, Kipnis E, Vela C, Chevallier S, Mallat J, Robert R; ABDOMIX Group. Early use of polymyxin B hemoperfusion in patients with septic shock due to peritonitis: a multicenter randomized control trial. Intensive Care Med. 2015 Jun;41(6):975-84. doi: 10.1007/s00134-015-3751-z. Epub 2015 Apr 11.
Results Reference
derived

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Effects of Hemoperfusion With a Polymyxin B Membrane in Peritonitis With Septic Shock

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