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2025-522349-23-00RecruitingPhase 3

Post-INFECT: Investigating Neuroinflammation and its effects in post-COVID syndrome

Post-INFECT: Investigating Neuroinflammation and its eFEcts in post-COVID syndrome: an imaging sTudy

Source: EU CTIS (euclinicaltrials.eu) · Last updated 1 Jun 2026

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Brief summary (registry, in English)

To assess differences between participants with persistent post-COVID complaints and controls without persistent post-COVID complaints in cellular metabolism in the brain as measured with dynamic [18F]FDG PET, structural and functional brain parameters as assessed with MRI, and immune-related blood parameters.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
65 (estimated)
First submitted
19 Feb 2026
Start date
5 Jul 2026
Lead sponsor
Amsterdam UMC Stichting
EU CT number
2025-522349-23-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 65
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The subject is actively using anti-inflammatory drugs

Other illness

  • The subject has an already known psychiatric, somatic or neurodegenerative condition that can explain his/her complaints

Other

  • The subject is unable to lay still for scanning due to claustrophobia, severe back pain or trypanophobia (fear of needles)
  • The subject is of female sex with childbearing potential and not surgically sterile, not refraining from sexual activity or not using reliable methods of contraception. Females of childbearing potential must orally and in writing confirm not to be pregnant or breastfeeding at the time of screening and at the day of the PET scan

Who the study is looking for

  • The subject was diagnosed with mild symptomatic COVID-19, confirmed by a positive PCR for SARS- CoV-2, positive SARS-CoV-2 serology or CO-RADS (COVID-19 Reporting and Data System) 4 or 5 on CT-scan, or antigen quicktest, or had typical symptoms and was part of a household in which another person was tested positive by PCR 2 weeks before or after the first day of illness
  • The subject is at least one year after being diagnosed with COVID-19
  • Subjects with persistent post-COVID complaints experience severe levels of fatigue (≥ 35) on the fatigue subscale of the Checklist Individual Strength [CIS-fatigue]) and/or difficulty concentrating (≥18) on the concentration subscale of the Checklist Individual Strength [CIS-concentration]. Control subjects without persistent complaints experiences no fatigue (<35) on the CIS-fatigue and no difficulty concentrating (<18) on the CIS-concentration
  • The subject is in the range 30-65 years of age
  • The subject has sufficient command of the Dutch language

Age in the registry: 18 years to 64 years · Sex: All · Accepts healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Amsterdam UMC StichtingAmsterdamNetherlandsRecruiting

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