CytoSorb SAH Trial

Emanuela Keller

Status: Terminated

Conditions: Aneurysmal Subarachnoid Haemorrhage

Treatments: Device: CytoSorb

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05259514

2021-D0082

Details and patient eligibility

About

In aSAH high levels of IL-6 (a pro-inflammatory cytokine) in the cerebrospinal fluid, as well as systemically have been linked to the severity grade and the occurrence of vasospasm and delayed cerebral ischemia caused by vasospasm as well as worse outcome independent of severity grade at time of admission and age. Increased levels of IL-6 increase the probability of unfavourable outcome, as well as the occurrence of delayed ischemic neurological deficit.

CytoSorb is an available, and certified medical device intended for use in conditions where elevated levels of cytokines such as IL-6 exist. Its clinical effect lies in the reduction of levels of pro-inflammatory mediators and thereby improving organ function as well as improving hemodynamic stability within hours of treatment initiation. Currently it is primarily used for the treatment of patients with confirmed or imminent respiratory failure who have either an acute lung injury, or acute respiratory distress syndrome, or a severe disease incl. respiratory failure, septic shock, and or multiple organ dysfunction/failure.

Until now, effective IL-6 removal in patients suffering from aSAH has not been possible in human and thus has not yet been evaluated. The purpose of this study is to see whether removal of IL-6 in patients with aSAH using CytoSorb is possible, and whether this alters the clinical course.

The overall goal of this study is to investigate whether a treatment with CytoSorb removes Interleukin 6 in patients with aSAH, and whether the treatment with CytoSorb alters the clinical course.

Full description

Study phase 1: patients (not randomized) will be allocated to the treatment group and compared to an already existing retrospective control group. The measurements and procedures are otherwise the same as in phase 2: Patients are randomized into a treatment group and a control group. In the treatment group the study intervention consists of the installation of a central venous line, connected to a device for hemoperfusion and removal of IL-6 using a CytoSorb Adsorber.

The overall objective is to evaluate efficacy, IL-6 levels will be measured daily in blood plasma as well as in cerebrospinal fluid between day 1 up to day 14 (routine procedure). Plasma and cerebrospinal fluid levels of IL-6 are evaluated using the routine samples. Furthermore, IL-6 will also be measured right after Cytosorb and the filtration to evaluate the amount of IL-6 that is actually removed by the filter (study-specific).

Only post-filter blood samples are taken for study purposes. Two post-filter blood samples (10-20ml totally) are taken for study purposes: first sample one hour after installation of CytoSorb and the second sample: 24 hours after installation.

Patient in the control group have standard of care treatment. The usual standard of care for the management of aneurysmal subarachnoid haemorrhage will be performed during the entire treatment period in both groups.

Enrollment: 2 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients (age ≥ 18years) admitted to the Neurointensive Care Unit (NICU)
• Subjects with aSAH with external ventricular drainage on admission computed tomography (CT) scan due to a ruptured aneurysm confirmed by digital subtracted angiography (DSA) or computed tomography based angiography (CTA), and successfully secured aneurysm by clipping or coiling within 3 days after aneurysm rupture
• Admission WFNS grade 4-5 (high-grade aSAH)
• A physician who is not participating in the research project is called in to safeguard the interests of the person concerned before he or she is involved in the project
• Informed Consent by signature from representative
• Informed Consent (post-hoc) by signature from patient, if possible

Exclusion criteria

• Subjects with moderate to severe vasospasm at time of admission as confirmed by CTA or DSA
• Any severe or unstable known inflammatory/immunodeficiency condition or disease (e.g. cancer, haematological, chronic infection or autoimmune disease) that might alter the natural inflammatory response
• Patients concurrently requiring immunosuppressive therapy, or who are profoundly immune suppressed
• Current infection with necessity of antibiotic treatment
• Any known coagulopathy or history of thromboembolic event leading to increased risk for thrombosis or bleeding
• Known allergies to polystyrene/divinylbenzene, polycarbonate, polypropylene, silicone and polyester
• Current pregnancy (as evaluated using a pregnancy test)
• Patients with very low platelet counts (< 20,000/μL).
• History of heparin-induced thrombocytopenia
• Acute sickle cell crisis
• Morbid obesity with BMI ≥ 40 kg/m2

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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2 participants in 2 patient groups

CytoSorb

Experimental group

Description:

Phase 2: 40 (20 each in treatment and control group). The Study Product is CytoSorb. Patients included will receive a CytoSorb filter. The device has a CE-mark and is used in accordance with its CE-Certification. Patients are installed as early as possible after exclusion of the bleeding source and are treated with the CytoSorb Adsorber for 48 hours. Blood flow will be set at least 200 ml/min.

Treatment:

Device: CytoSorb

Standard of Care

No Intervention group

Description:

Only routine treatment