Hyperdia: Hemodynamic Efficiency of an Hemodialysis Treatment With High Permeability in Post-resuscitation Shock

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Completed
CT.gov ID
NCT00780299
Collaborator
Gambro Industries, MEYZIEU, France (Other)
38
1
2
86
0.4

Study Details

Study Description

Brief Summary

Rationale: Despite spontaneous cardiac activity recovery, a shock occurs in more than half of patients after resuscitation for cardiac arrest. This acute circulatory insufficiency presents similar characteristics with septic shock and is responsible of most early deaths. Most frequently, usual treatments are unable to control this shock and to avoid the appearance of multiple organ failure.

Aim of the study: In addition to conventional therapeutics, an early plasma epuration of inflammatory mediators (HDHP) could be able to improve hemodynamic parameters and to reduce the shock duration. This improvement could have an impact on multiple organ dysfunctions and also on early mortality.

Condition or Disease Intervention/Treatment Phase
  • Device: hemodialysis with high permeability (HDHP)
  • Procedure: CVVH
Phase 3

Detailed Description

HDHP (plasma epuration of inflammatory mediators) will be used in addition to the current clinical practice. The experimental arm will be treated by HDHP device.

The high permeability membrane SepteX is a membrane polyarylethersulfone sold by Gambro that allows the purification of molecules of average size to near 50 kd molecular weight.

We can thus purify molecules larger molecular weight than hemofiltration can with the usual membranes (30 kd). Furthermore, this increase in permeability allows a significant treatment medium-sized molecules in diffusion (hemodialysis), that the usual membranes do not allow. Finally, it is possible to purify certain molecules that hemofiltration including high volume does not allow (TNFalpha for example).

Use of this membrane requires the use of specific set dedicated machine Prismaflex itself with a specific software (Exceed) to ensure the control and security of processing.

2 sessions of HDHP will be performed in the first 48 hours following ICU admission (with inclusion in the first 8 hours).

Study Design

Study Type:
Interventional
Actual Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Hemodynamic Efficiency of an Hemodialysis Treatment With High Permeability (HDHP) During the Early Period of Post-resuscitation Shock
Actual Study Start Date :
Nov 2, 2008
Actual Primary Completion Date :
Jan 2, 2016
Actual Study Completion Date :
Jan 2, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 2

control

Procedure: CVVH
hemofiltration intermittent dialysis

Experimental: 1

HDHP

Device: hemodialysis with high permeability (HDHP)
HDHP (hemodialysis with high permeability) is a specific plasma epuration of inflammatory mediators

Outcome Measures

Primary Outcome Measures

  1. The main endpoint will be the duration of the shock expressed by the length of catecholamine infusion [28 days]

Secondary Outcome Measures

  1. Changes in organ dysfunction score (SOFA, LOD) during the first 7 days Mortality at day 7 and day 28 Incidence of side effects and complications due to HDHP Impact of HDHP on inflammatory parameters. [28 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion criteria

  • Comatous patients admitted to the ICU for a sudden cardiac death apparently related to heart disease and requiring catecholamine infusion to treat a shock

  • Cardiac arrest in front of witnesses

  • Written informed consent obtained from the family or by emergency procedure

Exclusion criteria

  • Age under 18 years

  • Response to verbal commands (Glasgow score >7)

  • Terminal illness present before the cardiac arrest

  • Acquired or innate immune deficit

  • Anticoagulation not recommended or high hemorrhagic risk

  • pregnancy

  • weight > 100 kg

  • without social security

  • another clinical trial ongoing

  • cardiac arrest from non cardiac etiology

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical intensive care unit of Cochin-St Vincent de Paul university Hospital Paris France 75679

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Gambro Industries, MEYZIEU, France

Investigators

  • Principal Investigator: Alain Cariou, MD, PhD, Assistance Publique - Hôpitaux de Paris

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT00780299
Other Study ID Numbers:
  • P071005
First Posted:
Oct 27, 2008
Last Update Posted:
May 4, 2021
Last Verified:
Apr 1, 2021
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 4, 2021