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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02887807
Other study ID # 2012-753
Secondary ID
Status Withdrawn
Phase Phase 3
First received
Last updated
Start date January 2017
Est. completion date January 2019

Study information

Verified date March 2019
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cardiac arrest (CA) is a public health problem in industrialized countries. The prognosis of these patients remains poor with significant mortality and severe neurological sequelae in survivors.

The objective of the present study is to determine whether cyclosporine can improve patient clinical outcome after shockable CA. 520 patients with CA will be entered into a multicentre, randomized, placebo-controlled study. They will receive one single injection of cyclosporine (or placebo) prior to resuscitation. The incidence of the combined endpoint (mortality, irreversible brain damage informations such as bilateral abolition of N20 wave or absent motor response or extension to the nociceptive stimulation…) will be assessed 7 days after CA.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Witnessed out-of-hospital cardiac arrest

- Shockable cardiac rhythm at first medical contact (ventricular fibrillation, ventricular tachycardia)

Exclusion Criteria:

- Evidence of trauma

- Evidence of pregnancy

- Duration of no flow more than 30 minutes

- Rapidly fatal underlying disease

- Allergy to cyclosporin A

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Single intravenous bolus of cyclosporine A (2.5 mg/kg) at the onset of resuscitation
cardio-pulmonary resuscitation usual care of cardiac arrest
Single intravenous bolus of placebo at the onset of resuscitation
cardio-pulmonary resuscitation usual care of cardiac arrest

Locations

Country Name City State
France Hopital Cardiologique Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Combined incidence of all-cause mortality and irreversible brain damage status the presence of irreversible brain damage is defined by the bilateral abolition of the N20 wave on somatosensory evoked potentials recordings or the absence of motor response or extension to painful stimuli on the Glasgow Coma Scale. 7 days