Shockable Out of Hospital Cardiac Arrest Clinical Trial
— CYRUS IIOfficial title:
CYclosporine A in Shockable Out-of-hospital Cardiac Arrest ResUScitation
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Status | Withdrawn |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 |
Verified date | March 2019 |
Source | Hospices Civils de Lyon |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Withdrawn |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 |
Country | Name | City | State |
---|---|---|---|
France | Hopital Cardiologique | Bron |
Lead Sponsor | Collaborator |
---|---|
Hospices Civils de Lyon |
France,
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 |