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Multi-dimensional prediction of cardiotoxicity risk of anti-tuberculosis drugs and evaluation of the intervention effect of precise pharmaceutical services

Multi-dimensional prediction of cardiotoxicity risk of anti-tuberculosis drugs and evaluation of the intervention effect of precise pharmaceutical services

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115043
Enrollment
Unknown
Registered
2025-12-22
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Drug-resistant pulmonary tuberculosis

Interventions

Control group:Patients with drug-resistant pulmonary tuberculosis who received bedaquiline, lofazimine and moxifloxacin/levofloxacin treatment
TDM intervention group:TDM
Observation group:None

Sponsors

Ningbo First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with drug-resistant pulmonary tuberculosis (WHO 2020 criteria); 2.>= 18 Years old; 3.Accept regimens including bedaquiline, clofazimine, and moxifloxacin/levofloxacin Treatment; 4.Be willing to participate in the research;

Exclusion criteria

Exclusion criteria: 1.Pregnancy or pregnant woman; 2.Those who have recently participated in clinical trials of new drugs; 3.Previous history of heart disease; 4.Severe liver and kidney dysfunction; 5.Mental illness and inability to communicate Power;

Design outcomes

Primary

MeasureTime frame
Incidence of cardiotoxicity;

Secondary

MeasureTime frame
Economic evaluation;

Countries

China

Contacts

Public ContactXu HongBin

Ningbo First Hospital

jiang_rh@126.com+86 189 5178 3095

Outcome results

None listed

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