Long COVID registry in Navarre
Official title: Persistent COVID-19 Registry in Navarre. (Persicov-19)
Run by Fundacion Miguel Servet · NCT07417176 · Data updated 2026-11-12
This project will collect health and symptom information from people in Navarre who had confirmed COVID-19 and still have symptoms after 3 months to see how common and what kinds of lasting problems they have.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Fundacion Miguel Servet Academic / other |
| Locations | 1 site (Pamplona, Navarre) |
| Status | Recruiting |
| Started | January 4, 2021 |
| Main results expected | March 1, 2026 |
| Study ends | March 31, 2026 |
| Registry record updated | February 20, 2026 |
| Trial ID | NCT07417176 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are people in Navarre with a laboratory-confirmed SARS-CoV-2 infection who continue to report new or worsening symptoms present more than three months after the acute infection.
✕Probably not a fit
People whose persistent symptoms clearly predated their COVID-19 infection or who cannot attend the single required in-person visit at the study site are unlikely to receive benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational registry enrolling people with confirmed SARS-CoV-2 infection who report symptoms persisting more than three months. Investigators collect sociodemographic data (age, sex, ethnicity, smoking, comorbidities) and clinical/disease-management variables, including a checklist of persistent symptoms at a single visit. The goal is to determine the prevalence and medium- to long-term sequelae of COVID-19 in the Navarre population and to characterize patient subgroups. The registry is led by Fundación Miguel Servet and conducted at Hospital Universitario de Navarra in Pamplona.
Why it matters
Potential benefit: If successful, the registry could help clinicians and health planners better recognize common long COVID patterns and plan follow-up care and services for affected patients.
How similar studies have gone: Other hospital-based cohorts, such as the Carfi et al. cohort, have reported high rates of persistent symptoms after COVID-19, so this registry builds on existing observational findings rather than testing a novel therapy.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * History of confirmed SARS-CoV-2 infection * Presentation of symptoms that have persisted for more than 3 months after SARS-CoV-2 infection * The patient reports any of the symptoms listed in the clinical assessment questionnaire or checklist. Exclusion Criteria: * The symptom(s) referred to already existed prior to acute SARS-CoV-2 infection.
Where it's running
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Hospital Universitario de Navarra
Pamplona, Navarre, Spain Recruiting
Study contacts
- Principal investigator: Patricia Fanlo Mateo, MD, PhD — Hospital Universitario de Navarra. Pamplona. Spain
- Study coordinator: Ruth García Rey, SC
- Email: ruth.garcia.rey@navarra.es
- Phone: +3484822163
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.