Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07400848

Clinical Laboratory Evaluation, Assessment of Symptoms and Recovery in Patients With Post-COVID-19-Vaccination Syndrome

Led by University of Bern · Updated on 2026-05-05

200

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

U

University of Bern

Lead Sponsor

P

private practice Cell-Re-Active-Training in Bern

Collaborating Sponsor

AI-Summary

What this Trial Is About

Some people report persistent health problems after receiving the COVID-19 vaccine. These symptoms persist well beyond typical short-term vaccine side effects and are not attributable to any other known medical conditions. This condition is known as Post-Acute COVID-19 Vaccination Syndrome (PACVS). Symptoms can persist for months and affect several organ systems, causing issues such as fatigue, heart-related problems, neurological difficulties, and decreases in both physical ability and mental performance. PACVS shows similarities to Post-Acute COVID-19 syndrome (PACS) and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The biological processes that cause PACVS are still not fully understood. Recent research indicates that endothelial dysfunction, abnormalities in blood coagulation, and persistent inflammatory responses may contribute significantly to this process. However, it remains unclear how symptoms develop over time, which biological markers are associated with disease severity, and how these findings could support diagnosis and future treatment strategies. The CLEAR study is an observational research project designed to address these knowledge gaps by systematically documenting symptoms over time and investigating potential biological correlates in individuals affected by PACVS. The study consists of three complementary subprojects. The PROGRESS subproject aims to assess symptom burden, disease course, and patient-reported treatment experiences over an eight-month period using standardized questionnaires completed by participants. The ENDOCLOT subproject investigates whether individuals with PACVS show objective signs of endothelial dysfunction, abnormalities in blood clotting, and markers of systemic inflammation. Endothelial function will be evaluated through non-invasive vascular reactivity tests (EndoPAT), microscopic examination of blood cells, standardized platelet function assessments, and standard laboratory diagnostics. It further explores the correlation between these biological parameters and clinical symptom trajectories identified in PROGRESS. The REAL subproject examines the role of endothelial activation and the release of inflammatory signaling molecules (cytokines) in the development and persistence of PACVS. The main hypothesis of the CLEAR study is that PACVS is associated with measurable endothelial dysfunction, inflammatory activation, and coagulation abnormalities, and that these biological changes are related to symptom severity and persistence over time. By combining longitudinal symptom assessment with biological measurements, this study aims to improve understanding of PACVS and support the development of better diagnostic and therapeutic approaches in the future.

CONDITIONS

Official Title

Clinical Laboratory Evaluation, Assessment of Symptoms and Recovery in Patients With Post-COVID-19-Vaccination Syndrome

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Sufficient knowledge of German to complete study questionnaires and procedures
  • Coded participation with online consent confirmation (PROGRESS patients only)
  • Self-reported onset of persistent symptoms related to COVID-19 vaccination (PROGRESS patients only)
  • Willingness and ability to participate in an 8-month follow-up (PROGRESS patients only)
  • Signed informed consent (ENDOCLOT and REAL patients and controls)
  • Receipt of at least one COVID-19 vaccination (ENDOCLOT and REAL patients)
  • Onset of new, otherwise unexplained symptoms within 0-14 days after vaccination (ENDOCLOT and REAL patients)
  • Persistence of symptoms for at least 6 months after vaccination (ENDOCLOT and REAL patients)
  • Diagnosis of ME/CFS according to the Canadian Consensus Criteria and post-exertional malaise (ENDOCLOT and REAL patients)
  • For controls: History of COVID-19 vaccination without persistent side effects; age and sex matched to a patient
Not Eligible

You will not qualify if you...

  • Severe cognitive, physical, or psychiatric conditions that prevent participation
  • Active cancer or immunosuppressive disease
  • Known pregnancy at enrollment
  • Clinically suspected or confirmed COVID-19 infection after vaccination or near symptom onset
  • Pre-existing Long COVID symptoms
  • Recent or uncertain acute infections around vaccination time
  • Pre-existing medical conditions or medications that could explain symptoms (e.g., ME/CFS, POTS, fibromyalgia, autoimmune diseases)
  • Use of long-term, high-dose anti-inflammatory medications

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institute of Sport Science, University of Bern

Bern, Switzerland, 3012

Actively Recruiting

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Research Team

M

Mirko Schmidt, Prof. Dr.

CONTACT

M

Michaela Fux, PD Dr. phil. nat.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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