infectious aneurysm or artificial blood vessel infection after transplantation
Conditions
Interventions
Method
For the sample, dissolve 100 mg of rifampicin powder with stirring in 100 ml of 0.05 M phosphate buffer. Subsequently, add 100 mg of ascorbic acid + 490 mg of sodium chloride (for injection),
Sponsors
Oda Shinichiro
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The subjects to be studied should be patients diagnosed as infectious aneurysm or artificial blood vessel infection after artificial blood vessel transplantation.
Exclusion criteria
Exclusion criteria: Patients with history of allergy to rifampicin Patients who could not obtain consent from research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Major endpoints: control of infectious symptoms at 12 weeks postoperative Evaluate comprehensively with thermal clinical course, blood test data, CT etc image data | — |
Contacts
Public ContactTakuma Kobayashi
University Hospital, Kyoto Prefectural University of Medicine
Outcome results
None listed