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Post-market Safety Reassessment of Ulinastatin for Injection

Post-market Safety Reassessment of Ulinastatin for Injection

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006751
Enrollment
Unknown
Registered
2015-07-15
Start date
2014-08-01
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

All area

Interventions

general department:Ulinastatin Treat
ICU:Ulinastatin Treat

Sponsors

Center for ADR monitoring of Guangdong/Guangdong Pharmacological Society
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: Patients with ulinastatin treated

Exclusion criteria

Exclusion criteria: Not applicable

Design outcomes

Primary

MeasureTime frame
AE/ADR;

Countries

China

Contacts

Public ContactMingjuan Hua
huamj@techpool.com.cn+86 020-38972511

Outcome results

None listed

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