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NCT05224830: Hypercovid

Relationship Between Hyperventilation Syndrome and SARS-CoV-2 Infection

Completed Last updated 7 September 2022
What this trial tests

trial testing Nijmegen questionnaire score in COVID-19 in 2,846 participants. Completed in 1 July 2022.

Timeline
1 January 2021
Primary endpoint
1 May 2022
1 July 2022

Quick facts

Lead sponsorCentral Hospital, Nancy, France
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,846
Start date1 January 2021
Primary completion1 May 2022
Estimated completion1 July 2022
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Central Hospital, Nancy, France

Who can join

18 and older, any sex, with COVID-19 or Hyperventilation Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Is There a Relationship between Hyperventilation Syndrome and History of Acute SARS-CoV-2 Infection? A Cross-Sectional Study.
    Allado E, Poussel M, Hamroun A, Moussu A, et al · · 2022 · cited 4× · PMID 36360494 · DOI 10.3390/healthcare10112154

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Other recruiting trials for COVID-19

Currently open trials in the same condition.

Other Central Hospital, Nancy, France trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05224830.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing