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population pharmacokinetic study of immunosuppressive agents in patients with lung transplantation

population pharmacokinetic study of immunosuppressive agents in patients with liver transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029593
Enrollment
Unknown
Registered
2020-02-05
Start date
2020-02-01
Completion date
Unknown
Last updated
2020-02-10

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

Conditions

Lung transplantation

Interventions

Case series:None

Sponsors

Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 80 Years

Inclusion criteria

Inclusion criteria: 1) male or non-pregnant female lung transplant patients; 2) Any age; 3) first lung transplantation; 4) subjects with ideal concentration of tacrolimus treatment window and no intolerable adverse reactions; 5) those who can fully understand the purpose of the study and understand the possible adverse reactions, and who voluntarily participate in and sign the informed consent and have good compliance.

Exclusion criteria

Exclusion criteria: 1) occurrence of intolerable adverse reactions; 2) combined organ transplantation; 3) those who cannot be given tacrolimus orally; 4) accompanied with acute or chronic ulcers of the digestive system and serious gastrointestinal diseases; 5) patients receiving hemodialysis or peritoneal dialysis during the period; 6) any form of substance abuse or mental illness; 7) those with poor compliance; 8) participants in other clinical trials during the same period; 9) patients who are considered inappropriate for other reasons.

Design outcomes

Primary

MeasureTime frame
Trough concentrations;Liver and kidney function;body weight;CYP3A5 genotyping;

Countries

China

Contacts

Public ContactChen Jingyu

Wuxi People's Hospital

chenjy@wuxiph.com+86 0510-85351886

Outcome results

None listed

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