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Cytokine Adsorption in Patients With Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation

Cytokine Adsorption in Patients With Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation - Randomized, Controlled, Open-label Intervention, Multi-center Trial (CYCOV-II-study)

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04385771
Acronym
CYCOV-II
Enrollment
80
Registered
2020-05-13
Start date
2020-09-01
Completion date
2021-10-31
Last updated
2021-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronavirus Infection, COVID, Cytokine Storm, Extracorporeal Membrane Oxygenation, Respiratory Failure, SARS-CoV 2

Keywords

COVID-19, ECMO, ARDS, Cytokine Adsorption

Brief summary

In December 2019 in the city of Wuhan in China, a series of patients with unclear pneumonia was noticed, some of whom have died of it. In virological analyses of samples from the patients' deep respiratory tract, a novel coronavirus was isolated (SARS-CoV-2). The disease spread rapidly in the city of Wuhan at the beginning of 2020 and soon beyond in China and, in the coming weeks, around the world. Initial studies described numerous severe courses, particularly those associated with increased patient age and previous cardiovascular, metabolic and respiratory diseases. A small number of the particularly severely ill patients required not only highly invasive ventilation therapy but also extracorporeal membrane oxygenation (vv-ECMO) to supply the patient's blood with sufficient oxygen. Even under maximum intensive care treatment, a very high mortality rate of approximately 80-100% was observed in this patient group. In addition, high levels of interleukin-6 (IL-6) could be detected in the blood of these severely ill patients, which in turn were associated with poor outcome. From experience in the therapy of severely ill patients with severe infections and respiratory failure, we know that treatment with a CytoSorb® adsorber can lead to a reduction of the circulating pro- and anti-inflammatory cytokines and thus improve the course of the disease and the outcome of the patients. The aim of the study is to investigate the influence of extracorporeal cytokine adsorption on interleukin-6-levels and time to successful ECMO explantation under controlled conditions in patients with particularly severe COVID-19 disease requiring extracorporeal membrane oxygenation.

Detailed description

In December 2019, a series of unexplained cases of pneumonia in the city of Wuhan in China has come to light. In virologic analyses of samples from the patients' deep respiratory tract, a novel coronavirus was isolated (first named 2019-nCoV, then SARS-CoV-2). The disease spread rapidly in the city of Wuhan in early 2020 and soon beyond. On 30 January 2020, the Director-General of the World Health Organization (WHO) declared the outbreak a public health emergency of international concern, and on 11 March 2020, the World Health Organization declared the virus a pandemic. In humans, an infection with the virus can cause respiratory tract infections or even very severe pneumonia - these often end fatally, especially in old and pre-diseased patients. Due to the novelty of the virus, the data basis for therapy is very limited. To date, there are no clinical data for an effective specific therapy, nor is there a vaccination against the virus available, so that therapy, especially intensive care treatment for very severe courses, must concentrate only on supportive treatment of lung failure and other complications. The virus is highly contagious and infection results in a relevant number of deaths. Due to very uncertain data on the spread of the virus in the population, it is difficult to estimate the mortality rate - the case fatality rate is about 4% based on the known case numbers. In reports on the treatment of the first cases in Wuhan (Hubei Province, China) in January 2020, the need for intensive care treatment is described for about a quarter of the inpatient cases, 10-17% had to be ventilated invasively, and veno-venous extracorporeal membrane oxygenation (vv-ECMO) was necessary in 2-4% of the inpatient cases. Patients requiring ECMO have an extremely high mortality rate of 83-100% in the studies published, so far. In severe cases a pronounced release of vasoactive cytokines was repeatedly observed. Excessive release of these vasoactive mediators (cytokine storm) can result in severe vasodilatation and membrane leakage, which can ultimately lead to vasoplegic shock that is difficult to control. Ruan et al. and Zhou et al. have identified high interleukin 6 (IL-6) levels as a potential predictor of a fatal outcome when compared between survivors and patients who died of COVID-19 disease. IL-6 is also an important factor in the pathophysiology of severe septic shock and excessive immune response in hemophagocytic lymphohistiocytosis (HLH) - for both indications has been shown, that the extracorporeal adsorption of IL-6 and other vasoactive substances in a CytoSorb® adsorber (CytoSorbents Corporation, Monmouth Junction, NJ, USA) leads to a significant reduction of these cytokines in the patient blood. Clinical experience and (previously unpublished) data from our monocentric registry study show that cytokine adsorption in a CytoSorb® Adsorber can also be safely integrated into a vv-ECMO system.

Interventions

in COVID-19-diseased vv-ECMO patients additional treatment with cytokine adsorption using a Cytosorb adsorber will be randomized (vs. control group)

COVID-19-diseased treated with vv-ECMO

Sponsors

Klinikum Ibbenbüren
CollaboratorUNKNOWN
Ludwig-Maximilians - University of Munich
CollaboratorOTHER
University Hospital, Saarland
CollaboratorOTHER
Klinikum Ludwigsburg
CollaboratorOTHER
University of Ulm
CollaboratorOTHER
SLK Kliniken Heilbronn GmbH
CollaboratorOTHER
Martin-Luther-Universität Halle-Wittenberg
CollaboratorOTHER
Dr. Alexander Supady
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

randomized controlled trial examining COVID-patients requiring vv-ECMO therapy (+/- cytokine adsorption)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* SARS-CoV-2-infection with COVID-pneumonia * vv-ECMO therapy

Exclusion criteria

* known patient will against participation in the study or against the measures applied in the study * a decision (made prior to inclusion of the patient into this trial) to terminate the treatment within the next 24 hours

Design outcomes

Primary

MeasureTime frameDescription
IL-6 reduction by 75% or more after 72 hours as compared to the baseline measurement72 hoursmeasurement of IL-6 levels in patient blood after 72 hours of cytokine adsorption (in relation to level before initiation of cytokine adsorption)
time to successful ECMO-explantation30 daystime to successful ECMO-explantation within 30 days after randomization

Secondary

MeasureTime frameDescription
Overall survival time30 daysOverall survival time, defined as time from randomization to death. The time will be censored at the time of last visit for surviving patients.
Days on intensive care unit (ICU)30 daysDays on intensive care unit (ICU)
Vasopressor dosage24, 48, 72 hoursVasopressor dosage of adrenaline, noradrenaline, vasopressin, and dobutamine at 24, 48,72 h
Fluid substitution and fluid balance24, 48, 72 hoursTotal fluid\[ml\] substitution and fluid balance \[ml\] at 24, 48, 72 h
Serum lactate24, 48, 72 hoursSerum lactate at 24, 48, 72 h
Urine output24, 48, 72 hoursUrine output at 24, 48, 72 h
Willebrand factor24, 48, 72 hoursWillebrand factor at 24, 48, 72 h
Ventilator free days (VFD)30 daysVentilator free days (VFD) in the first 30 days after randomization, where invasive mechanical ventilation (IMV), non-invasive ventilation (NIV) and ECMO are defined as ventilator days. VFD=0, if the patient dies in the first 30 days after randomization
interleukin-6 levels24, 48, 72 hoursinterleukin-6 levels at 24, 48, 72 h
SOFA-Score24, 48, 72 hoursSequential Organ Failure Assessment Score at 24, 48, 72 h (values from 6 to 24, where the higher values explain higher disease severity)
serious adverse device effects30 daysserious complications or malfunctions related to the CytoSorb device
adverse event of special interest: air in the ECMO system30 daysunintended air in the ECMO system during operation of the device
adverse event of special interest: blood-clotting in the ECMO system30 daysunintended blood-clotting in the ECMO system during operation of the device
adverse event of special interest: bleeding complications30 daysmajor bleeding events
d-dimers24, 48, 72 hoursd-dimers at 24, 48, 72 h
Time to extubation from ventilation and explantation from ECMO30 daysTime to extubation from ventilation and explantation from ECMO. Death under ventilation and/or ECMO will be analyzed as a competing event. The time will be censored at the time of last visit for surviving patients under ventilation and/or ECMO.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026