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Study on the impact of Canagliflozin combined with chemotherapy on the outcomes of patients with pulmonary tuberculosis and diabetes mellitus comorbidity

Study on the impact of Canagliflozin combined with chemotherapy on the outcomes of patients with pulmonary tuberculosis and diabetes mellitus comorbidity

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118444
Enrollment
Unknown
Registered
2026-02-05
Start date
2026-02-15
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Pulmonary Tuberculosis

Interventions

Experimental group:Use canagliflozin to lower blood sugar
Control group:Use other hypoglycemic drugs

Sponsors

Tongji University Affiliated Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Subject age: 18 years old <= age <= 75 years old, both male and female are eligible; 2. Subject weight: 40 kg <= weight <= 90 kg; 3. Patients with newly diagnosed, drug-sensitive pulmonary tuberculosis combined with type 2 diabetes; 4. HIV test negative; 5. Non-pregnant and non-lactating women, agree to continue using contraception throughout the study; 6. Fully understand the purpose and requirements of this trial and voluntarily sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. HIV-positive patients; 2. Patients with sputum culture indicating non-tuberculous mycobacteria (NTM); 3. Confirmed hepatobiliary diseases, including but not limited to chronic active hepatitis and/or liver dysfunction, HBsAg positive with high viral load (Hepatitis B e antigen positive), AST or ALT >3 times the upper limit of normal, TBIL >2 times the upper limit of normal; 4. The following history of kidney disease or kidney-related manifestations: unstable or rapidly progressive kidney disease; moderate/severe renal impairment or end-stage renal disease (eGFR = 133 µmol/L; female Cr >= 124 µmol/L).

Design outcomes

Primary

MeasureTime frame
conversion rate of sputum culture;Cure rate;

Secondary

MeasureTime frame
Changes in blood inflammatory markers;

Countries

China

Contacts

Public ContactSha Wei

Tongji University Affiliated Shanghai Pulmonary Hospital

shfksw@126.com+86 136 7175 8200

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026