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A clinical observational cohort study of cough after novel coronavirus infection

A clinical observational cohort study of cough after novel coronavirus infection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072082
Enrollment
Unknown
Registered
2023-06-02
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

novel coronavirus infection

Interventions

Patients with novel coronavirus infection:no

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18-80 years old. (2) The patient has had a positive result of nucleic acid test or antigen self-test of novel coronavirus or a history of COVID-19 related epidemiology. (3) Cough lasted for more than 3 weeks. (4) Patients must sign informed consent before being enrolled in the cohort, and can participate in the study protocol and follow up according to the protocol.

Exclusion criteria

Exclusion criteria: (1) A history of asthma with a definite diagnosis. (2) Used systemic corticosteroids, ICS or ICS combined with LABA, or ICS combined with LABA+LAMA during the four weeks prior to enrollment; Or acute respiratory tract infection; Or lung CT with significant lung inflammation. (3) Serious systemic diseases or chronic respiratory diseases with clear diagnosis in the past, such as heart failure, kidney failure, liver failure (the underlying disease is stable, and the original medication regimen should be maintained as long as the drug is maintained), COPD, cystic fibrosis, bronchiectasis, interstitial lung disease, tuberculosis, lung cancer, etc. (4) Patients who have known significant risk factors for cough, including, but not limited to, the use of ACEI/ARB drugs. (5) Women of childbearing age who are currently pregnant or lactating. (6) Received immunosuppressive therapy or participated in clinical investigators 3 months before enrollment.

Design outcomes

Primary

MeasureTime frame
cough evaluation test, CET;Leicester Cough Questionnaire, LCQ;VAS;

Secondary

MeasureTime frame
lung function;airway inflammation;

Countries

China

Contacts

Public ContactLiu Yi

Shandong Provincial Hospital

yiliu_sdu@163.com+86 151 6888 8626

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026