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Efficacy of Colchicine in the prevention and treatment of Interstitial lung disease in patients with COVID-19

Efficacy of Colchicine in the prevention and treatment of Interstitial lung disease in patients with COVID-19

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067948
Enrollment
Unknown
Registered
2023-02-01
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

COVID-19

Interventions

experimental group:Standard treatment+Colchicine
control group:Standard treatment

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age= 18 years old; (2) Inpatient treatment in the Second Hospital of Lanzhou University; (3) Positive COVID-19 nucleic acid test within 24 hours; (4) Combined with = 2 of the following clinical manifestations:?fever (body temperature >37.3 °C);? persistent cough;?persistent dry throat and sore throat;?muscle soreness;?loss or loss of smell and/or taste;?General symptoms of viral influenza such as nasal congestion, runny nose, headache, fatigue, etc.;?Increased breathing (respiratory rate> 25 times/min;? Reduced blood oxygen saturation (<95%)? (5) Chest CT showed viral pneumonia. (6) Female patients are not fertile (at least 1 year after menopause or sterilization) or fertile but use effective contraceptive methods. (7) Voluntary signing of informed consent: Patients and their families voluntarily sign the informed consent form after the investigator informs the investigator of the study-related matters in person, indicating that they voluntarily participate in the study and can comply with the requirements of the study follow-up plan and other protocols.

Exclusion criteria

Exclusion criteria: (1) Pregnant and lactating women. (2) Those who are allergic to constitution or multiple drugs (3) Those with a history of liver cirrhosis, chronic active hepatitis, severe liver disease or severe liver insufficiency (Child-Pugh grade C). (4) Severe renal insufficiency (estimated GFR 450 milliseconds. (7) Those with low bone marrow hyperplasia. (8) Those with colchicine and other indications (such as: gout, familial Mediterranean fever) are being treated. (9) Those who are participating in other clinical trials. (10) Those who refuse to accept the study or cannot cooperate for any reason.

Design outcomes

Primary

MeasureTime frame
Incidence of ILD;Warrick score;

Secondary

MeasureTime frame
Lung function parameters;arterial partial pressure of oxygen;Warrick score of chest CT;SF-36 score;Murray lung injury score;adverse event;

Countries

China

Contacts

Public ContactZhang Sigong

Lanzhou University Second Hospital

zhangsg@lzu.edu.cn15809310299

Outcome results

None listed

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