Safety Study of Inhaled Carbon Monoxide to Treat Acute Respiratory Distress Syndrome (ARDS)

Acute Respiratory Distress Syndrome (ARDS) Clinical Trial

Official title:

A Phase I Trial of Inhaled Carbon Monoxide for the Treatment of Sepsis-Induced Acute Respiratory Distress Syndrome (ARDS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02425579
• Other study ID #: 1408015437
• Status: Completed
• Phase: Phase 1
• Start date: April 2015
• Est. completion date: August 2019

Study information

• Verified date: October 2019
• Source: Brigham and Women's Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the safety of inhaled carbon monoxide (iCO) in intubated patients with sepsis-induced ARDS.

Description:

The acute respiratory distress syndrome (ARDS) is a syndrome of severe acute lung inflammation and hypoxemic respiratory failure with an incidence of 180,000 cases annually in the U.S.Despite decades of research and recent advances in lung protective ventilator strategies, morbidity and mortality remain unacceptably high. Furthermore, no specific effective pharmacologic therapies currently exist. The lack of specific effective therapies for sepsis-related ARDS indicates a need for new treatments that target novel pathways. Carbon monoxide (CO) represents a novel therapeutic modality in ARDS based on data obtained in experimental models of ARDS and sepsis over the past decade.

CO has been shown to be protective in experimental models of Acute Lung Injury (ALI), including hyperoxia and endotoxin exposure, bleomycin, ischemia/reperfusion, and ventilator-induced lung injury (VILI). At low doses, CO has been shown to confer tissue protective effects in these ALI models. In addition, CO has been shown to decrease inflammation, enhance phagocytosis, and improve mortality in models of sepsis including endotoxemia, hemorrhagic shock, and cecal ligation and puncture (CLP). CO has also been shown to have beneficial therapeutic effects in pre-clinical models of disease including pulmonary hypertension, vascular injury, and transplantation. Furthermore, multiple human studies have demonstrated that experimental administration of several different concentrations of CO is well tolerated and that low dose inhaled CO can be safely administered to subjects in a controlled research environment.

The purpose of this study is to assess the safety of inhaled CO therapy in mechanically ventilated patients with sepsis-induced ARDS.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: August 2019
• Est. primary completion date: August 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients with sepsis are defined as those with suspected or documented infection:

Suspected or proven infection: Sites of infection include thorax, urinary tract, abdomen, skin, sinuses, central venous catheters, and central nervous system

All eligible patients meet the new definition of sepsis (suspected or proven infection and a SOFA = 2) as PaO2/FiO2 ratio < 300 = 2 SOFA points.

2. ARDS is defined when all four of the following criteria are met:

• A PaO2/FiO2 ratio = 300 with at least 5 cm H2O positive end-expiratory airway pressure (PEEP)

• Bilateral infiltrates consistent with pulmonary edema on frontal chest radiograph

• A need for positive pressure ventilation by an endotracheal or tracheal tube

• No clinical evidence of left atrial hypertension for bilateral pulmonary infiltrates.

3. ARDS onset is defined as the time the last of criteria 1-4 are met. ARDS must persist through the enrollment time window of 120 hours.

4. Infiltrates considered "consistent with pulmonary edema" include any infiltrates not fully explained by mass, atelectasis, or effusion or opacities known to be chronic (greater than 1 week). Vascular redistribution, indistinct vessels, and indistinct heart borders alone are not considered "consistent with pulmonary edema" and thus would not count as qualifying opacities for this study.

Exclusion Criteria:

1. Age less than 18 years

2. Greater than 120 hours since ARDS onset

3. Pregnant or breast-feeding

4. Prisoner

5. Patient, surrogate, or physician not committed to full support (exception: a patient will not be excluded if he/she would receive all supportive care except for attempts at resuscitation from cardiac arrest)

6. No consent/inability to obtain consent

7. Physician refusal to allow enrollment in the trial

8. Moribund patient not expected to survive 24 hours

9. No arterial line/no intent to place an arterial line

10. No intent/unwillingness to follow lung protective ventilation strategy

11. Severe hypoxemia defined as oxygenation saturation (SpO2) <95 or PaO2 <80 on FiO2 =0.8

12. Hemoglobin < 7.5 g/dl or hemoglobin < 8 g/dl and actively bleeding

13. Subjects who are Jehovah's Witnesses or are otherwise unable or unwilling to receive blood transfusions during hospitalization

14. Acute myocardial infarction (MI) or acute coronary syndrome (ACS) within the last 90 days

15. Coronary artery bypass graft (CABG) surgery within 30 days

16. Angina pectoris or use of nitrates with activities of daily living

17. Cardiopulmonary disease classified as New York Heart Association (NYHA) class IV

18. Stroke (ischemic or hemorrhagic) within the prior 3 months

19. Diffuse alveolar hemorrhage from vasculitis

20. Use of high frequency ventilation

21. Participation in other interventional studies involving investigational agents

22. Burns > 40% total body surface area

23. Use of inhaled pulmonary vasodilator therapy (eg. NO or prostaglandins)

Related Conditions & MeSH terms

• Acute Lung Injury
• Acute Respiratory Distress Syndrome (ARDS)
• Respiratory Distress Syndrome, Adult
• Respiratory Distress Syndrome, Newborn
• Syndrome

Intervention

Drug:
• Inhaled Carbon Monoxide at 100ppm (4 participants)
Inhaled Carbon Monoxide at 100ppm for up to 90 minutes daily for 5 days
• Placebo for Inhaled Carbon Monoxide at 100ppm (2 participants)
Inhaled Medical Air for up to 90 minutes daily for 5 days
• Inhaled Carbon Monoxide at 200ppm (4 participants)
Inhaled Carbon Monoxide at 200ppm for 90 minutes daily for 5 days
• Placebo for Inhaled Carbon Monoxide at 200ppm (2 participants)
Inhaled Medical Air for up to 90 minutes daily for 5 days

Locations

Country	Name	City	State
United States	Brigham and Women's Hospital	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	Duke Univesity Hospital	Durham	North Carolina
United States	Weill Cornell Medical College/NewYork-Presbyterian	New York	New York

Sponsors (4)

Lead Sponsor	Collaborator
Brigham and Women's Hospital	Duke University, Massachusetts General Hospital, Weill Medical College of Cornell University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Plasma biomarkers of inflammation, lung epithelial injury,endothelial injury, markers of change in other end-organ function	Specific Biomarkers: Plasma biomarkers of inflammation (IL-6, IL-8, IL-10, IL-1 receptor antagonist (IL-1Ra), IL-18, IL-1ß, and circulating mitochondrial DNA), lung epithelial injury (RAGE), endothelial injury (vWF, Ang-2), markers of change in other end-organ function (e.g., creatinine, liver function tests, lactate)	5 days
Primary	Number of administration associated adverse events.	Acute myocardial infarction (MI) within 48 hours of study drug administration; Acute cerebrovascular accident (CVA) within 48 hours of study drug administration; New onset atrial or ventricular arrhythmia requiring direct current (DC) cardioversion within 48 hours of study drug administration; Increased oxygenation requirements defined as: an increase in fraction of inspired oxygen (FiO2) of greater than or equal to 0.2 AND increase in PEEP greater than or equal to 5 cm of water (H2O) within 6 hours of study drug administration; Increase in any protocol-specified measurement of carboxyhemoglobin (COHb) greater than or equal to 10%; Increase in lactate by greater than or equal to 2 mmol/L within 6 hours of study drug administration	60 Days if remains in the ICU
Primary	Incidence of serious adverse events (SAEs).	An SAE is any event that is fatal or immediately life threatening, is permanently disabling, or severely incapacitating, or requires or prolongs inpatient hospitalization. Important medical events that may not result in death, be life threatening, or require hospitalization may be considered SAEs when, based upon appropriate medical judgment, they may jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the outcomes listed above.	60 Days if remains in the ICU
Secondary	Comparison between the calculated carboxyhemoglobin (COHb) level at 90 minutes using the Coburn-Forster-Kane (CFK) equation and measured COHb level at 90 minutes	The Coburn-Forster-Kane (CFK) equation will be used to calculate the estimated COHb level at 90 minutes for Cohorts 1 and 2.	5 days
Secondary	Mean daily Sequential Organ Failure Assessment (SOFA) score	Organ failure will be assessed using the SOFA score. SOFA scores will be assessed daily on days 1-5, and day 7, as the SOFA score has been shown to be a reliable prognostic indicator of outcomes in critically ill patients.	7 days
Secondary	Partial pressure of arterial oxygen (PaO2)/FiO2 ratio	PaO2/FiO2 will be measured daily on days 1-5 if a subject remains mechanically ventilated.	5 days
Secondary	Oxygenation index (OI)	The OI will be measured daily on days 1-5 if a subject remains mechanically ventilated.	5 days
Secondary	Lung injury score (LIS)	The LIS is a composite 4-point scoring system including the PaO2/FiO2, PEEP, quasi-static respiratory compliance, and the extent of infiltrates on the chest X-ray. Previous randomized clinical trials in ARDS have shown that a decreased LIS correlates with improvement in lung physiology as well as important clinical outcomes including mortality and ventilator-free days (VFDs).	7 Days
Secondary	Vasopressor-free days	Ventilator-free days will be assessed on day 28.	28 days
Secondary	Ventilator-free days (VFDs)	Ventilator-free days to day 28 are defined as the number of days from the time of initiating unassisted breathing to day 28 after randomization, assuming survival for at least two consecutive calendar days after initiating unassisted breathing and continued unassisted breathing to day 28. If a subject returns to assisted breathing and subsequently achieves unassisted breathing to day 28, VFDs will be counted from the end of the last period of assisted breathing to day 28.	28 days
Secondary	ICU-free days	ICU-free days will be assessed on day 28.	28 days
Secondary	Hospital-free days	Hospital-free days will be assessed on day 60.	60 days