Mystery illness after COVID shot? new study seeks answers
NCT ID NCT07400848
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at people who have long-lasting health problems after getting the COVID-19 vaccine, a condition called Post-Acute COVID-19 Vaccination Syndrome (PACVS). Researchers will track symptoms over eight months and test blood and blood vessel function to find biological clues. The goal is to better understand why symptoms persist and help develop better diagnosis and treatments in the future. About 200 adults are needed for this observational study.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Progress:The study aims to enrol approximately 150-200 adults (≥18 years) who report persistent and severe symptoms following COVID-19 vaccination. Endoclot/Real: The study includes 40 individuals with suspected PACVS who meet criteria for ME/CFS and PEM, as identified through the PROGRESS subproject. Each patient is matched with a healthy control of similar age (±10 years) and sex. Control participants must have received a COVID-19 vaccination but report no persistent adverse effects and no chronic illness.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
General Criteria (apply to all study parts: PROGRESS, ENDOCLOT, REAL, patients and matched healthy controls) Inclusion Criteria 1. Age ≥ 18 years 2. Sufficient knowledge of German to complete study-related questionnaires and procedures Exclusion Criteria 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) Inclusion Criteria 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 Exclusion Criteria 1\. No specific exclusion criteria for this part ENDOCLOT and REAL (patients and matched healthy controls) Inclusion Criteria 1. Signed informed consent form 2. For patients: 1. Receipt of at least one COVID-19 vaccination 2. Onset of new, otherwise unexplained symptoms within 0-14 days after vaccination 3. Persistence of symptoms for at least 6 months following vaccination 4. Selection is based on a diagnosis of ME/CFS according to the Canadian Consensus Criteria (CCC) and PEM. 2\. For controls: History of COVID-19 vaccination without persistent adverse effects; age (+/- 10 years), and sex match to a corresponding case Exclusion Criteria (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 3. Any self-reported or uncertain history of an acute infectious event (including mild or subclinical infections) in temporal proximity to COVID-19 vaccination 4. Known pre-existing medical conditions or ongoing medications that could plausibly explain the reported symptoms (e.g., preexisting ME/CFS, POTS, fibromyalgia, small-fiberneuropathy, autoimmune disease with systemic involvement or other chronic multisystemic dysautonomia syndromes) 5. Use of long-term, high-dose anti-inflammatory
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Institute of Sport Science, University of Bern
RECRUITINGBern, 3012, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.