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Systematic Early Use of Neuromuscular Blocking Agents in ARDS Patients
This study has been completed.
Sponsors and Collaborators: Assistance Publique Hopitaux De Marseille
GlaxoSmithKline
Information provided by: Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier: NCT00299650
  Purpose

The use of neuromuscular blocking agents (NMBA) in ARDS patients has not been extensively investigated. The aim of the study is to show a reduction of the mortality rate of ARDS patients.


Condition Intervention Phase
ARDS
Drug: cisatracurium
Drug: Placebo
Drug: Cisatracurium besilate
Phase IV

MedlinePlus related topics: Pneumonia
Drug Information available for: Cisatracurium Cisatracurium besylate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Systematic Early Use of Neuromuscular Blocking Agents in ARDS Patients

Further study details as provided by Assistance Publique Hopitaux De Marseille:

Primary Outcome Measures:
  • Reduction of the mortality rate of ARDS patients at d90 [ Time Frame: 36 months ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Mortality at day 28, day 60, day 180 and ICU mortality, Ventilator-free days and alive at day 28 and day 60, Exposure time to FIO2 > 80% or PEEP > 10 cmH2O during the first 7 days, Sedatives and analgesics requirements during the first 7 days [ Time Frame: march 2009 ] [ Designated as safety issue: Yes ]
  • Organ failure-free days and alive at day 28, Incidence of barotrauma, Incidence of critical illness neuromyopathy, Incidence of ventilator-associated pneumonia, Quality of life at day 180 [ Time Frame: march 2009 ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 340
Study Start Date: March 2006
Study Completion Date: October 2008
Primary Completion Date: October 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
A: Placebo Comparator Drug: Placebo
physiological serum infusion
B: Active Comparator Drug: cisatracurium Drug: Cisatracurium besilate
Cisatracurium besilate infusion (900mg/day)

Detailed Description:

The use of neuromuscular blocking agents (NMBA) in ARDS patients has not been extensively investigated. It has been recently demonstrated that a systematic 48-h infusion of NMBA is associated with a significant improvement in oxygenation as compared with a control group (Gainnier et al., Crit Care Med 2004). Moreover, a trend towards a reduction in the mortality rate has been observed. The aim of the study is to show a reduction of the mortality rate of ARDS patients.

  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ARDS with a PaO2 / FiO2 < 150 with a PEEP > 5 since less than 48 hrs
  • informed consent

Exclusion Criteria:

  • NMBA allergy
  • Continuous administration of NMBA for ARDS prior inclusion
  • Age < 18 yrs
  • SAPS II > 70
  • Persistent air leak
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00299650

Locations
France
Hôpital Sainte-Marguerite - Réanimation médicale
Marseille, France, 13009
Réanimation Polyvalente - Hôpital Sainte-Marguerite
Marseille, France, 13009
Hôpital Nord - Réanimation
Marseille, France, 13015
Hôpital Ambroise Paré - Réanimation
Marseille, France, 13000
Hôpital Saint-Louis - Réanimation médicale
Paris, France
Hôpital Jean Minjoz - Réanimation médicale
Besancon, France
Hôpital Pontchaillou - Réanimation médicale
Rennes, France
Réanimation médicale
Brest, France
Hôpital Pellegrin - Réanimation médicale
Bordeaux, France, France
Hôpital de la croix rousse - Réanimation médicale
Lyon, France
Réanimation chirurgicale
Montpellier, France
Hôpital Bellevue - Réanimation Médicale
Saint-Etienne, France
Réanimation chirurgicale
Clermont-Ferrand, France
Réanimation Polyvalente
Avignon, France
Réanimation polyvalente
Aix en Provence, France
Réanimation polyvalente
Toulon, France
Réanimation médicale
Nice, France
Réanimation Médicale
Nimes, France
Réanimation chirurgicale
Nimes, France
Hôpital de la Tronche - Réanimation médicale
Grenoble, France
Sponsors and Collaborators
Assistance Publique Hopitaux De Marseille
GlaxoSmithKline
Investigators
Principal Investigator: Laurent Papazian, MD Assistance Publique Hôpitaux de Marseille
  More Information

Responsible Party: ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE ( Pr PAPAZIAN Laurent )
Study ID Numbers: ACURASYS, PHRC 2004
Study First Received: March 6, 2006
Last Updated: October 9, 2008
ClinicalTrials.gov Identifier: NCT00299650  
Health Authority: France: Ministry of Health

Keywords provided by Assistance Publique Hopitaux De Marseille:
ARDS
mortality
mechanical ventilation
pneumonia
muscle relaxants

Study placed in the following topic categories:
Cisatracurium
Muscle Hypotonia
Atracurium
Pneumonia

Additional relevant MeSH terms:
Neuromuscular Nondepolarizing Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Cholinergic Antagonists
Nicotinic Antagonists
Physiological Effects of Drugs
Neuromuscular Agents
Neuromuscular Blocking Agents
Peripheral Nervous System Agents
Cholinergic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009