Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

Cytokine filtration in lung transplantation

Official title: Cytokine Filtration in Lung Transplantation - a Randomised, Controlled, Multicentre Clinical Trial (GLUSorb)

Run by Lund University Hospital · NCT05526950 · Data updated 2026-11-12

This study is testing whether using a special device to filter out harmful substances during lung transplants can help patients have fewer complications and live longer.

More Lung Transplant Failure trials

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment116 (estimated)
SponsorLund University Hospital
Academic / other
Locations1 site (Lund, Skåne County)
StatusRecruiting
StartedSeptember 7, 2023
Main results expectedDecember 31, 2027
Study endsDecember 31, 2029
Registry record updatedSeptember 18, 2023
Trial IDNCT05526950 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals eligible for double lung transplantation who meet the study's inclusion criteria.

Probably not a fit

Patients under 18 years old, those with previous organ transplants, or those requiring immunosuppressive therapy at the time of surgery may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the use of cytokine adsorption devices in lung transplantation to reduce early complications such as primary graft dysfunction (PGD). It is a randomized controlled trial comparing outcomes in patients receiving lung transplants with and without the cytokine filtration intervention. The goal is to gather preliminary data on the efficacy of this approach in improving patient survival and reducing complications associated with lung transplants. The study focuses on the inflammatory response that occurs immediately after transplantation and aims to mitigate its effects.

Why it matters

Potential benefit: If successful, this approach could significantly improve survival rates and reduce complications for lung transplant recipients.

How similar studies have gone: Previous studies in heart and kidney transplantation have shown success with cytokine adsorption, suggesting potential for similar outcomes in lung transplantation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

• Eligibility to undergo double lung transplantation at either trial site

Exclusion Criteria:

1. Age \<18 years
2. Previous organ transplantation
3. Presence of any conditions at the time of surgery that require immunosuppressive therapy. Immunosuppressive therapy is defined as:

   1. Cyclosporine, Tacrolimus, Everolimus, or Sirolimus, minimum 1 month of treatment prior to transplantation and active treatment at the time of transplantation.
   2. Any form of antibody-based treatment that is known for having an immunomodulatory effect taken up to 1 week before transplantation.
4. Non-consent

Where it's running

  • Sandra Lindstedt
    Lund, Skåne County, Sweden
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Multimodal prospective approach to understand acute and chronic lung transplant rejection

    This project will see if blood tests, airway sampling, imaging, and genetic analyses can identify which adults who have had or are being evaluated for a lung transplant will develop antibody‑mediated rejection and later chronic graft dysfunction.

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  • Airway response to exercise after double lung transplant

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.