TTrialPathMatch Me to Trials
← Back to trials
RecruitingPost-Acute COVID-19 Vaccination SyndromePostviral Fatigue

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

Eligible age

18+ yrs

Accepts

All genders

Locations

0 states

Healthy volunteers

Yes

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

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.

Sponsor: University of Bern

You may qualify if…

  • ✓ 1. Age ≥ 18 years
  • ✓ 2. Sufficient knowledge of German to complete study-related questionnaires and procedures
  • ✓ 1. Coded participation with online consent confirmation
  • ✓ 2. Self-reported onset of persistent symptoms temporally associated with a COVID-19 vaccination
  • ✓ 3. Willingness and ability to participate in the 8-month follow-up period
  • ✓ 1. Signed informed consent form
  • ✓ 2. For patients:
  • ✓ 1. Receipt of at least one COVID-19 vaccination

You may not qualify if…

  • ✕ 1. Severe cognitive, physical impairment or psychiatric conditions impeding participation
  • ✕ 2. Active oncological disease or immunosuppressive
  • ✕ 3. Known pregnancy at the time of enrolment
  • ✕ PROGRESS (patients only)
  • ✕ 1\. No specific exclusion criteria for this part
  • ✕ ENDOCLOT and REAL (patients and matched healthy controls)
  • ✕ 1. Clinically suspected or laboratory confirmed SARS-CoV-2 infection after vaccination or temporally related to symptom onset.
  • ✕ 2. Concurrent pre-existing Long COVID symptoms, obtained from the patient´s history

Source: ClinicalTrials.gov · NCT07400848 · last updated 2026-05-05