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Inflammatory ResponseROCKSTARNCT06286280

Removal Of CytoKines With cytoSorbenTs After Inflammatory Response Reaction During Cardiac Surgery

A study testing cytokine adsorber (CytoSorb®) in people with Inflammatory Response, run by University of Giessen at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Detailed knowledge about the association between systemic inflammation and endothelial progenitor cell (EPCs) activation during extracorporeal circulation (ECC) is lacking. This pilot study aims to clarify the relationship between CD34-positive EPCs and cytokine release during ECC using the cytokine adsorber to make a… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Inflammatory Response
What is being tested?
cytokine adsorber (CytoSorb®)
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteGermany
Study dates
1 May 2023to 27 Mar 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • planned cardiac surgical procedure with the use of the cardiopulmonary machine as well as with ECMO use (elective or urgent)
  • age at the time of surgery of \>18 years.
  • informed consent

Who cannot join

  • An emergency indication;
  • endocarditis, a non-sterile inflammation,
  • autoimmune diseases, chronic inflammatory diseases (ankylosing spondylitis, psoriasis, rheumatoid arthritis, chronic inflammatory intestinal diseases), an acquired immune deficit (HIV);
  • severe liver dysfunction, hepatitis B/0;
  • patients on dialysis;
  • Patients with a hematopoietic disorder/tumour disease;
  • participation in other interventional trials or studies;
  • timely and probable follow-up cannot be guaranteed (e.g. due to long distances between home and study site); a pregnancy that cannot be excluded with certainty (no menopause, no sterilization).

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Universityhospital Giessen, Department of Cardiovascular Surgery

    Giessen, Germany, 35392

Other trials in Germany

About this study

Official title: Removal of Cytokines With Cytosorbents After Inflammatory Response Reaction During Cardiac Surgery and Association of Endothelial Progenitor Cells

Detailed knowledge about the association between systemic inflammation and endothelial progenitor cell (EPCs) activation during extracorporeal circulation (ECC) is lacking.

This pilot study aims to clarify the relationship between CD34-positive EPCs and cytokine release during ECC using the cytokine adsorber to make a predictive statement regarding the clinical expression of inflammation.

Read the detailed description

Mechanical cardiovascular support procedures are used as part of cardiac surgery. Here, heart-lung machines (HLM) and miniaturized systems such as ECMO (extracorporeal membrane oxygenation) are used to replace cardiac and/or pulmonary function. Contact with non-physiologic artificial surfaces can induce a generalized 'sterile' inflammatory syndrome called SIRS (Systemic Inflammatory Response Syndrome). During SIRS, proinflammatory cytokine release occurs due to complement activation. These massively released, diverse cytokines significantly influence the activation and release of endothelial progenitor cells (EPCs) from the bone marrow during extracorporeal circulation (ECC) and their long-term functionality.

The life-threatening complications of the so-called cytokine storm can potentially be avoided with the help of a cytokine adsorber (CytoSorb®), and the stabilization process after the hyperinflammatory phase can be promoted. However, it is unclear the quantitative and qualitative modification of the cytokine expression pattern by the use of the cytokine adsorber and its influence on the release of EPCs as well as on the clinical course of the patients. Although a therapy extension with cytokine adsorber has a positive impact on the reduction of cytokine levels in the blood, cytokine removal has not been investigated in direct correlation to EPCs.

These interactions are to be investigated within the scope of the proposed project.

This project is a pilot study with a translational science background to clarify the relationship between CD34-positive endothelial progenitor cells and cytokine release in the setting of ECCs using cytokine adsorber. Previous studies have shown a positive association between increased cytokine levels and the number of circulating endothelial progenitor cells. To date, it has not been investigated how this correlation or association changes with the use of cytokine adsorbers. Therefore, due to the specificity of targeted cytokine removal, the findings obtained here may provide essential insights in basic clinical research that could be applied to clinical issues and decision-making processes in the future. Due to the increasingly important role of extracorporeal circulatory support systems, detailed knowledge of the relationship between systemic inflammation and endothelial progenitor cell activation during their use will be increasingly important in the future.

The current project aims to investigate whether an association between the inflammatory response during and after cardiac surgery and the number of stem cells (EPCs) continues to exist when the cytokine adsorber (CytoSorb®) is applied and whether and how the adsorber can influence the functionality, migratory capacity, and differentiation of stem cells. We assume that under these conditions, a direct correlation of EPCs with inflammation does not exist, so a modulation of the SIRS (Systemic Inflammatory Response Syndrome) clinically observed by us could be absent. In addition, we will investigate whether a correlation between the number of circulating endothelial progenitor cells (CD 34+ cells) and the concentration of cytokines can be observed to make a predictive statement regarding the clinical expression of inflammation.

The long-term goal is to identify patients at high risk for clinical manifestations of inflammation after using the EPC and, based on the knowledge gained, make a predictive statement based on the concentration pattern of the EPC.

This prospective study should provide information on whether and at which point perioperative hyperinflammation can be reliably predicted and whether establishing a specific cytokine adsorber could positively influence the number of EPCs and, thus, short- and medium-term survival.

Being tested
cytokine adsorber (CytoSorb®)
Keywords
CD34+ endothelial progenitor cells, systemic inflammation, extracorporeal circulation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cytokine adsorber (CytoSorb®)Device

    binding of cytokines to the sorbent polystyrene of the adsorber during cardiac surgery with extracorporeal circulation

Study groups in NCT06286280
Study groupRoleWhat they receive
Cytosorb groupExperimentalUse of hemoadsorber for removal of cytokines. Participants undergoing cardiac surgery will be treated using a hemoadsorption device (CytoSorb) within the cardiopulmonary Bypass circuit (=Intervention)
Receives: Device: cytokine adsorber (CytoSorb®)
Control groupNo interventionParticipants undergoing cardiac surgery will be treated according to Standard of care (no hemoadsorption advice installed in the CPB circuit)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. correlation of endothelial progenitor cells with cytokine levels with and without adsorber use

    How does the number of EPCs during adsorber use correlate with cytokine levels, and how does the adsorber influence the time course of EPC release (measurement before and after adsorber use)?

    Measured: 24 hours before until day 7 post-surgery

Secondary outcomes (6)
  1. Overall mortality rate

    Overall mortality rate until day 30

    Measured: until day 30 post surgery

  2. Days on ventilator, vasopressor and renal replacement therapy

    Total days on ventilator, vasopressor and renal replacement therapy within 30 days post-surgery will be assessed

    Measured: until day 30 post-surgery

  3. incidence of stroke

    incidence of stroke within 30 days post-surgery will be assessed

    Measured: until day 30 post-surgery

  4. length of ICU and in-hospital stay

    total length of ICU and in-hospital stay until day 30 post-surgery

    Measured: until day 30 post-surgery

  5. Echocardiographic changes

    Does a cytokine adsorber influence left ventricular function?

    Measured: 24 hours before until day 7 post-surgery

  6. Influence of Cytokine on endothelial progenitor cells

    Does a cytokine adsorber influence EPC function? After isolation (CD34 sorting) and cultivation in stem cell medium, EPCs will be functionally characterized using angiogenesis assays (sprouting assay; tube formation), migration assays and measurement of DiI-Ac-LDL uptake.

    Measured: 24 hours before and immediately after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Feb 2024
  2. Study start1 May 2023
  3. Primary completion1 Dec 2024
  4. Study completion27 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Model description
single-center, two-arm randomized-controlled prospective study
Masking
Single blind
Who is masked
Participant
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06286280
Sponsor's protocol ID
AZ221/21
Other IDs
F/23/22
Acronym
ROCKSTAR
Status last verified
Mar 2024
First submitted
22 Feb 2024
Last updated
6 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing cytokine adsorber (CytoSorb®) in people with Inflammatory Response, run by University of Giessen at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

correlation of endothelial progenitor cells with cytokine levels with and without adsorber use (time frame: 24 hours before until day 7 post-surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Apr 2025.

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