Clinical study on biliary infection therapy :A RCT on clinical efficacy of DRPM in biliary tract infection with IPM/CS as comparator

Clinical study on biliary infection therapy :A RCT on clinical efficacy of DRPM in biliary tract infection with IPM/CS as comparator - Clinical study on biliary infection therapy

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000003852

Enrollment

120

Registered

2010-07-01

Start date

2010-06-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Acute biliaring infection

Interventions

DRPM IPM/CS

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Acute biliary infection

Exclusion criteria

Exclusion criteria: 1)History of hypersensitivity to DRPM 2)Serious complications 3)Serious cardiac disfunctions 4)Serious renal disfunctions 5)With CNS disorder 6)History of hypersensitivity to B-lactam antibiotics 7)Pregnant or lactating women and women who may be pregnant 8)MRSA infection 9)Judged by investigator not to be appropriate for inclusion in this study

Design outcomes

Primary

Measure	Time frame
Clinical effectiveness	—

Secondary

Measure	Time frame
Clinical effectiveness at 3,7days Safety(moniterd clinical and laboratory evaluation)	—

Countries

Japan

Contacts

Public ContactSusumu Tazuma

graduate school of biomedicalscience, Hiroshima university. Department of General Medicine

stazuma@hiroshima-u.ac.jp082-257-5461

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026