Actively Recruiting
Prospective Cohort Study Investigating Vaccine-Induced Immune Responses Against Respiratory Viral Infections in Immunocompromised Patients With or Without Hematological Conditions
Led by University of Cologne · Updated on 2026-05-12
1000
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the immune responses to vaccines against respiratory viruses in immunocompromised patients, including those with hematological or oncological conditions. These patients often have weakened immune systems due to disease or treatment, making them more vulnerable to severe respiratory infections from viruses like influenza, RSV, and coronaviruses. The study aims to better understand how vaccine-induced immunity, especially T cell responses, functions in these patients, as current data mostly focuses on antibody responses which may be less effective in this group. This observational study will analyze early and late booster vaccinations in immunocompromised patients who are vaccinated as part of routine care. It will focus on measuring virus-specific T cell responses and humoral immune responses over time. The research will gather blood samples and other data to assess the cellular and antibody responses to vaccination, helping to fill knowledge gaps about long-term protection in this vulnerable population. Participants will be monitored for up to 12 months after vaccination to evaluate humoral and cellular immune responses, including seroconversion. The study will collect and analyze samples at various points to measure these immune markers. The University of Cologne leads this research, which seeks to improve understanding of vaccine effectiveness and guide better preventive strategies for immunocompromised patients facing respiratory viral infections.
CONDITIONS
Brief Title
Vaccine-induced Immunity in Immunocompromised Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent form
- Patients with immunosuppression caused by treatment or underlying diseases
- Patients who have been vaccinated or are willing to be vaccinated against respiratory virus infections according to current recommendations
- Age 18 years or older
You will not qualify if you...
- Patients unwilling or ineligible for vaccination under current recommendations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 months
Participants who undergo routine vaccination and care are observed for immune responses to respiratory virus vaccines.
Multiple visits for sample collection and immune response assessments
Trial Site Locations
Total: 1 location
1
University Hospital Cologne
Cologne, North Rhine-Westphalia, Germany, 50937
Actively Recruiting
Research Team
S
Sibylle Mellinghoff, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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