Post-Covid Condition Cohort: Evolution of Symptomatology, Patient Profile and Associated Prognostic Factors
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentral Hospital, Nancy, France
About this trial
The aim of our cohort is to collect prospectively, in a standardized and exhaustive manner, the health data of patients referred to the CAPCoV, our holistic referal post covid clinics for post-covid condition in order to be able to identify typical profiles of patients suffering from post covid syndrome and to follow the evolution of their disease over time.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
outpatients treated in the Nancy University Hospital Long Covid Support and Care Center for post-Covid condition according to WHO definition
Disqualifiers
patient opposing the processing for research purposes of their data collected in routine care for their care
Trial population
outpatients treated in the Nancy University Hospital Long Covid Support and Care Center for post-Covid condition according to WHO definition
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Symptoms
Symptoms collected in a standardized manner during consultations, their persistence over time, their evolution (improvement, stagnation, worsening) and their severity (mild, moderate, severe)
Time frame
every 6 months up to 3 yearsSecondary outcomes
1
Medical history
Time frame
baseline2
fatigue
Chalder scale: range 0 to 33, \>22/33 classified severe
Time frame
every 6 months up to 3 years3
Dyspnea
mMRC
Time frame
every 6 months up to 3 years4
Cognitive impairement
Montréal Cognitive Assessment : range 0 to 30, \<26/30 classified pathologic
Time frame
every 6 months up to 3 yearsSponsors and contacts
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Source ClinicalTrials.gov