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Clinical trial of atorvastatin adjunctive therapy in pulmonary tuberculosis

Clinical trial of atorvastatin adjunctive therapy in pulmonary tuberculosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104959
Enrollment
Unknown
Registered
2025-06-26
Start date
2025-07-20
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

Tuberculosis

Interventions

Control Group:Standard Treatment

Sponsors

Huzhou Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-75 years; 2.Radiographic findings consistent with pulmonary tuberculosis; 3.Sputum smear-positive for acid-fast bacilli (AFB) with GeneXpert confirmation of rifampicin-sensitive Mycobacterium tuberculosis; 4.Planned standard anti-TB treatment with 2HRZE/4HR regimen; 5.Willing to comply with study procedures and follow-up.

Exclusion criteria

Exclusion criteria: 1.Previous history of anti-tuberculosis treatment; 2.Pulmonary TB with concurrent extrapulmonary TB involvement; 3.Known hypersensitivity to atorvastatin or its excipients; 4.History of myopathy or hereditary muscle disorders; 5.Hepatic failure or decompensated cirrhosis; 6.Hypothyroidism (uncontrolled); 7.HIV infection; 8.Pregnant or lactating women; 9.Current use of immunosuppressive medications; 10.Use of any statin within 3 months prior to screening; 11.Conditions requiring long-term statin therapy based on cardiovascular risk: Familial hypercholesterolemia History of myocardial infarction or stroke; 12.Laboratory abnormalities at screening: ALT >5× upper limit of normal (ULN) eGFR 5× ULN Serum potassium <2.5 mmol/L; 13.Any other severe comorbidities deemed by investigators to compromise patient safety or study validity.

Design outcomes

Primary

MeasureTime frame
culture conversion rate;

Secondary

MeasureTime frame
Adverse Event;radiographic assessment;

Countries

China

Contacts

Public ContactQingqiu Zeng

Huzhou Center Hospital

zeng2116@163.com+86 572 2555409

Outcome results

None listed

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