Cohort study on the evolution of symptoms and profiles in post-COVID patients
Post-Covid Condition Monitoring Cohort: Evaluation of the Evolution of Symptomatology, Patient Profile and Associated Prognostic Factors
Central Hospital, Nancy, France · NCT05610436
This study is trying to learn more about how symptoms change over time in people dealing with long COVID by collecting health information from patients at a special clinic.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Central Hospital, Nancy, France (other) |
| Locations | 1 site (Vandœuvre-lès-Nancy, Grand Est) |
| Trial ID | NCT05610436 on ClinicalTrials.gov |
What this trial studies
This observational cohort aims to systematically collect health data from patients referred to the CAPCoV clinic at Nancy University Hospital, focusing on those experiencing post-COVID conditions. The study will identify typical patient profiles and track the progression of symptoms over time. By gathering comprehensive data, the research seeks to enhance understanding of long COVID and its associated prognostic factors.
Who should consider this trial
Good fit: Ideal candidates include outpatients treated for post-COVID conditions at the Nancy University Hospital Long Covid Support and Care Center.
Not a fit: Patients who oppose the use of their routine care data for research purposes will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management and treatment strategies for patients suffering from long COVID.
How similar studies have performed: While there have been various studies on long COVID, this cohort approach focusing on patient profiles and symptom evolution is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * outpatients treated in the Nancy University Hospital Long Covid Support and Care Center for post-Covid condition according to WHO definition Exclusion Criteria: * patient opposing the processing for research purposes of their data collected in routine care for their care
Where this trial is running
Vandœuvre-lès-Nancy, Grand Est
- Nancy University Hospital — Vandœuvre-lès-Nancy, Grand Est, France (RECRUITING)
Study contacts
- Principal investigator: Francois GOEHRINGER, MD — Infectious Diseases Department, Nancy University Hospital,F-54000 Nancy, France.
- Study coordinator: Francois GOEHRINGER, MD
- Email: francois.goehringer@chru-nancy.fr
- Phone: +33383154097
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Long COVID, Post-Acute COVID-19, Post-Acute COVID19 Syndrome