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The Concentration Monitoring of Safty for ShuXueNing TCM Injection

The Concentration Monitoring of Safty for ShuXueNing TCM Injection

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006649
Enrollment
Unknown
Registered
2015-06-26
Start date
2015-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

ADR

Interventions

none:shuxuening tcm injection

Sponsors

Tianjin University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 100 Years

Inclusion criteria

Inclusion criteria: all the patients who accept the treatment of shuxuening injection

Exclusion criteria

Exclusion criteria: the patients who allergic to shuxuening injection.

Design outcomes

Primary

MeasureTime frame
ADR;

Countries

China

Contacts

Public Contactzhangjunhua
zjhtcm@foxmail.com+86 022 27412619

Outcome results

None listed

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