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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05224830
Other study ID # 2021PI224-203
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date July 1, 2022

Study information

Verified date February 2022
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Following an acute COVID-19 infection, many patients suffer from long lasting physical symptoms that may greatly impair quality of life. Persisting dyspnea and other functional respiratory complaints could evoke Hyperventilation Syndrome (HVS) as a putative contributor of the long-COVID presentation in COVID-19 survivors. We aimed to assess the possible relationship between a HVS and previous acute SARS-CoV-2 infection.


Recruitment information / eligibility

Status Completed
Enrollment 2846
Est. completion date July 1, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Read and speak French - Perform a pulmonary function test Exclusion Criteria: - incomplete questionnaire or inability to obtain an interpretable lung function assessment

Study Design


Intervention

Other:
Nijmegen questionnaire score
We collected the Nijmegen Questionnaire in order to diagnosis of Hyperventilation Syndrome

Locations

Country Name City State
France Centre Hospitalier Régional Universitaire de Nancy. Vandoeuvre les nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess the relationship between a hyperventilation syndrome and previous acute SARS-CoV-2 infection. Nijmegen questionnaire during 15 minutes (cross-sectional monocentric study)
Secondary Assess the relationship between a hyperventilation syndrome and dyspnea Nijmegen questionnaire during 15 minutes (cross-sectional monocentric study)
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