Pilot Study of Sodium Nitrite in Resuscitated Cardiac Arrest Patients
Primary Purpose
Cardiac Arrest
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
nitrite
Sponsored by
About this trial
This is an interventional treatment trial for Cardiac Arrest focused on measuring cardiac arrest, ventricular fibrillation, nitrite
Eligibility Criteria
Inclusion Criteria:
- Successfully resuscitated from cardiac arrest by paramedics in the field Age 18 or older Comatose IV access
Exclusion Criteria:
- traumatic cause of cardiac arrest known DNAR Patient requiring vasopressors at time of randomization SBP <105 PaO2 of less than 90% on FiO2 of 1.0
Sites / Locations
- Harborview Medical Center
Outcomes
Primary Outcome Measures
Blood pressure
nitrite concentration levels in blood
Secondary Outcome Measures
Full Information
NCT ID
NCT01178359
First Posted
August 6, 2010
Last Updated
May 16, 2017
Sponsor
University of Washington
Collaborators
Medic One Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01178359
Brief Title
Pilot Study of Sodium Nitrite in Resuscitated Cardiac Arrest Patients
Official Title
Phase 1 Hospital Based Study of Sodium Nitrite in Resuscitated Cardiac Arrest Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Medic One Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Despite advances in cardiac arrest resuscitation survival from cardiac arrest is less than 20-30% and new therapies are urgently needed. Sodium nitrite infused during resuscitation from cardiac arrest has recently been shown to improve survival in a mouse model of cardiac arrest and our group is eager to test this hypothesis in a clinical trial. Our overall hypothesis is that an infusion of 2 μmole/kg sodium nitrite during resuscitation will increase the proportion of patients who will survive cardiac arrest. In preparation for a clinical trial, preliminary safety and efficacy data (phase 1) is needed which is the primary goal of this study.
Detailed Description
Sixteen patients will be randomized to receive normal saline (n=5) or doses of IV nitrite (n=11). During the nitrite infusion and for 120 min after the infusion is completed, blood pressure and heart rate will be monitored.
The first 3 patients randomized to receive IV nitrite will receive the lowest dose (1 mg) of IV nitrite and compared to one placebo treated patient. If there is no significant decrease in blood pressure or elevation in heart rate, we will then dose escalate to the 6 mg dose in 4 patients and placebo in two patients. Dose escalation to the highest (14 mg) dose will again be contingent on the absence of significant hypotension or tachycardia in the drug treated patients compared to the pooled (n=3) placebo treated patients. The final block of patients will be randomized to the high nitrite dose (n=4) or placebo (n=2). Final comparisons of all groups will be made to the pooled (n=5) placebo group
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest
Keywords
cardiac arrest, ventricular fibrillation, nitrite
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
nitrite
Primary Outcome Measure Information:
Title
Blood pressure
Time Frame
2 hour
Title
nitrite concentration levels in blood
Time Frame
2 hour
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Successfully resuscitated from cardiac arrest by paramedics in the field Age 18 or older Comatose IV access
Exclusion Criteria:
traumatic cause of cardiac arrest known DNAR Patient requiring vasopressors at time of randomization SBP <105 PaO2 of less than 90% on FiO2 of 1.0
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis Kim, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harborview Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Pilot Study of Sodium Nitrite in Resuscitated Cardiac Arrest Patients
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