Post-Covid Condition Cohort: Evolution of Symptomatology, Patient Profile and Associated Prognostic Factors

Recruiting

• Conditions: Post-Acute COVID19 Syndrome; Long COVID; Post-Acute COVID-19

• Registration Number: NCT05610436
• Lead Sponsor: Central Hospital, Nancy, France

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-01-07
• Status Verified: 2022-10
• Study First Submitted: 2022-10-20
• Study First Submitted QC: 2022-11-08
• Last Update Submitted: 2022-11-08
• Study First Posted: 2022-11-09
• Last Update Posted: 2022-11-09
• Primary Completion: 2025-12
• Study Completion: 2026-06

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 500

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Symptoms	every 6 months up to 3 years	Symptoms collected in a standardized manner during consultations, their persistence over time, their evolution (improvement, stagnation, worsening) and their severity (mild, moderate, severe)

Secondary Outcome Measures

Name	Time	Method
Cognitive impairement	every 6 months up to 3 years	Montréal Cognitive Assessment : range 0 to 30, \<26/30 classified pathologic
additional examinations	every 6 months up to 3 years	Biology, imaging
Medical history	baseline
inappropriate hyperventilation syndrome	every 6 months up to 3 years	Nijmegen score: range 0 to 64, \>23/34 classified "possible inapropriate hyperventilation" syndrome"
fatigue	every 6 months up to 3 years	Chalder scale: range 0 to 33, \>22/33 classified severe
Dyspnea	every 6 months up to 3 years	mMRC

Trial Locations

Locations (1)

Nancy University Hospital; 🇫🇷 Vandoeuvre les nancy, Grand Est, France