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NCT06951321

Characteristics of Postinfectious Cough

Completed Last updated 30 April 2025
What this trial tests

trial in Cough in 1,650 participants. Completed in 1 April 2025.

Timeline
1 March 2023
Primary endpoint
1 April 2025
1 April 2025

Quick facts

Lead sponsorKefang Lai
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,650
Start date1 March 2023
Primary completion1 April 2025
Estimated completion1 April 2025
Sites1 location across China

Conditions studied

Sponsor

Kefang Lai

Who can join

Adults 18 to 70, any sex, with Cough. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Collect the age, sex and other demographic data of 1600 patients with chronic cough after COVID-19 infection and clinical parameters such as cough characteristics, establish a cohort of patients with chronic cough after COVID-19 infection, observe the type and level of airway inflammation, airway responsiveness, cough sensitivity and changes in microbiology of patients with chronic cough after COVID-19 infection, clarify the epidemiological characteristics, clinical pathophysiological characteristics, long-term prognosis and related factors of patients with chronic cough after COVID-19 infection, explore the clinical pathophysiological characteristics and pathogenesis of cough after COVID-19 infection, and provide a theoretical basis for the treatment of persistent cough after COVID-19 infection.

Publications & conference data

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

  1. Long-Term Prognosis of Adult Patients with Persistent Cough Post COVID-19 and Its Risk Factors: A Nationwide Prospective Study.
    He W, Zhang J, Sun D, Yi F, et al · · 2026 · PMID 41848877 · DOI 10.1007/s00408-026-00879-x

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Other recruiting trials for Cough

Currently open trials in the same condition.

Other Kefang Lai trials

Trials by the same sponsor.

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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/NCT06951321.

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