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A multicentre clinical trial of Lianhua Qingke tablet in the treatment of medium-size novel coronavirus infection

A multicentre clinical trial of Lianhua Qingke tablet in the treatment of medium-size novel coronavirus infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074231
Enrollment
Unknown
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Moderate novel coronavirus infection

Interventions

experimental group:Basic treatment add Lianhua cough clearing tablets
control group:Basic treatment add placebo control

Sponsors

Qilu Hospital of Shandong University (Qingdao)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The diagnostic criteria are consistent with the diagnostic criteria for moderate COVID-19 infection. 2.Over 18 years of age (including 18 years of age), male or female. 3.Have cough symptoms. 4.Written informed consent is signed voluntarily by the patients participating in this clinical trial before enrollment.

Exclusion criteria

Exclusion criteria: 1.Patients who have other respiratory diseases (e.g., chronic obstructive pulmonary disease, tumors, tuberculosis) or whose cough or phlegm symptoms are determined by the investigator to be caused by other diseases (e.g., pneumoconiosis, pulmonary abscess, bronchiectasis, cough variant asthma, eosinophilic bronchitis, or upper airway cough syndrome) or whose cough symptoms are caused by medications. 2.Patients with serious primary diseases of the heart, brain, lung, liver, kidney and hematopoietic systems, as well as mental diseases. 3.Allergic constitution (allergic to more than 2 types of substances), or allergic to the composition of this preparation. 4.Alanine aminotransferase (ALT), aspartate aminotransferase (AST) >5× upper limit of normal (ULN). 5.Pregnant, lactating and pregnant women. 6.Participants in other drug clinical trials within the past 1 month. 7.A suspected or existing history of alcohol or drug abuse, or other conditions or conditions that, in the investigator's judgment, reduce or complicate enrollment.

Design outcomes

Primary

MeasureTime frame
Rate of disappearance of cough symptoms;

Secondary

MeasureTime frame
Improvement rate of CT examination;Pulse oxygen monitoring(In the state of inhaled air);Proportion of turning severe or critical;

Countries

China

Contacts

Public ContactDing Meiling

Qilu Hospital of Shandong University (Qingdao)

18561811909@163.com+86 185 6181 1909

Outcome results

None listed

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