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Study for permeability of tigecycline in lung tissue of patients with pulmonary infection

Study for permeability of tigecycline in lung tissue of patients with pulmonary infection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017478
Enrollment
Unknown
Registered
2018-08-01
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

pulmonary infection

Interventions

Conventional dose group:Load dose: 100mg, ivgtt
maintenance dose: 50mg, q12h, ivgtt
High dose group:Load dose: 200mg, ivgtt
maintenance dose: 100mg, q12h, ivgtt

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Subjects use clinically recognized and up-to-date diagnostic criteria, clinically diagnosed by clinical symptoms, signs, laboratory and X-ray examinations for patients with bacterial lung infections who require antimicrobial therapy; (2) According to the standard principle of empirical treatment or pathogen test results, the pathogen is shown in the antibacterial spectrum of tigecycline; (3) The effective antibacterial drug has not been used within 72 hours before the subject is selected, or the antibacterial drug has not been used; (4) Aged at least 18 years old, male and female; (5) The subject has no serious liver, kidney, cardiovascular and hematopoietic diseases; (6) Patients of childbearing age are willing to take appropriate methods of contraception; (7) The subject is an inpatient; (8) Voluntary subjects and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who are known or suspected to be allergic to tigecycline or tetracycline antibiotics or have serious adverse reactions; (2) Patients who have received any other test medications during the first three months of screening or enrollment; (3) Patients who are being treated with cyclosporine and warfarin; (4) Patients who have been selected for clinical trials of this study drug; (5) Patients with other diseases that the study believes will not be able to evaluate efficacy or are unlikely to complete the expected course of treatment and visits; (6) Patients with severe liver damage (Child Pugh grade C); (7) Women during pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
plasma concentration of tigecycline;bronchoalveolar lavage fluid concentration of tigecycline;

Secondary

MeasureTime frame
serum concentration of urea;bronchoalveolar lavage fluid concentration of urea;

Countries

China

Contacts

Public ContactYang Yong

Sichuan Provincial People's Hospital

yyxpower@163.com+86 13981843406

Outcome results

None listed

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