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Association of proton pump inhibitors with renal adverse events in non-small cell lung cancer patients treated with PD-1 Inhibitor (APPIANI Study)

Association of proton pump inhibitors with renal adverse events in non-small cell lung cancer patients treated with PD-1 Inhibitor (APPIANI Study)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057366
Enrollment
Unknown
Registered
2022-03-09
Start date
2022-04-01
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

acute kidney disease and renal dysfunction

Interventions

exposure group:using PPIs
control gruop:without PPIs

Sponsors

The Third Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnose as non-small cell lung cancer stage III-IV; 2. Treatment with PD-1 inhibitors; 3. Age between 18-65 years old; 4. Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Autoimmune diseases, such as systemic lupus erythematosus, Sjogren's syndrome, vasculitis, etc; 2. Basic renal disease (abnormal urine detection, such as urine protein or urine occult blood, or estimated glomerular filtration rate<60ml/min/1.73m2; 3. History of major allograft organ transplantation, especially kidney transplantation; 4. For gastrointestinal diseases, proton pump inhibitors must be used for a long time; 5. Have a history of heart failure, angina, severe arrhythmia or pericardial disease; 6. Infectious diseases, including active hepatitis B or C, syphilis, acquired immunodeficiency syndrome (AIDS); 7. Serious infectious diseases; 8. The expected survival time is less than half a year; 9. Mental disorders, including clinically defined depression and schizophrenia; 10. Any other situation that may limit the patient's ability to participate in the study.

Design outcomes

Primary

MeasureTime frame
AKD: kidney injury within 3 months, including AKI;

Countries

China

Contacts

Public ContactMin Yang

The Third Affiliated Hospital of Soochow University, Changzhou 213003

yangmin1516@suda.edu.cn+86 519 68872083

Outcome results

None listed

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