Clinical Trials Directory

Trials / Completed

CompletedNCT05954325

Immunoadsorption vs. Sham Treatment in Post COVID-19 Patients With Chronic Fatigue Syndrome

Extracorporal Apheresis Hannover Medical School Study in Post COVID-19 Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Hannover Medical School · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The complex clinical symptoms of post COVID syndrome, especially chronic fatigue, pose a major challenge to patients and to the health care system and are frequently refractory to therapeutic intervention. There is increasing evidence that a dysregulated post-viral immune response may be involved in the pathogenesis of post COVID syndrome. In uncontrolled case studies, an improvement of fatigue symptoms after removing autoantibodies has been reported in post COVID patients. However, there is a lack of prospective, sham controlled studies. We initiate an interventional, randomised, sham treatment-controlled prospective study, the EXTINCT post COVID study, which aims to scientifically test the therapeutic efficacy of an extracorporeal apheresis procedure (immunoadsorption) for the treatment of a well characterized cohort of patients with post COVID syndrome, while at the same time providing basic research evidence for an understanding of the pathogenesis of post COVID syndrome. Thereby, we expect to obtain important insights into the diagnosis, treatment and pathophysiology of post-COVID syndrome.

Conditions

Interventions

TypeNameDescription
PROCEDUREImmunoadsorption vs. sham immunoadsorption5 treatments within 14 days

Timeline

Start date
2023-08-15
Primary completion
2025-07-31
Completion
2025-07-31
First posted
2023-07-20
Last updated
2025-09-15

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT05954325. Inclusion in this directory is not an endorsement.