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Post-Market Safety Reassessment of Safflower and Aceglutamide Injection

Post-Market Safety Reassessment of Safflower and Aceglutamide Injection

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031123
Enrollment
Unknown
Registered
2020-03-22
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-03-23

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

Conditions

All area

Interventions

case series:Safflower and Aceglutamide Injection

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All inpatients in the monitored hospitals who received Safflower And Aceglutamide Injectionby intravenous drip.

Exclusion criteria

Exclusion criteria: Not applicable

Design outcomes

Primary

MeasureTime frame
AE/ADR;

Countries

China

Contacts

Public ContactSong Yanqing
yangqingyjk@163.com+86 15843079687

Outcome results

None listed

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