A real-world study on the clinical application and safety of monkshood

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400084580

Enrollment

Unknown

Registered

2024-05-21

Start date

2024-06-11

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

No fixed disease

Interventions

Case series :N/A

Eligibility

Sex/Gender

All

Age

No minimum to 100 Years

Inclusion criteria

Inclusion criteria: 1.Those who take traditional Chinese medicine decoctions containing aconite after clinical diagnosis and treatment; 2.Hospitalized patients; 3.The patient voluntarily participated in this study and signed a written informed consent form, willing to cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1.For external use of traditional Chinese medicine decoctions containing aconite; 2.Patients with concomitant mental illness; 3.Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
effectiveness;	—

Countries

China

Contacts

Public ContactLi Fangyuan

Shenzhan Bao'an Chinese Medicine Hospital

lifangyuan89@gzucm.edu.cn+86 131 2895 3354

Outcome results

None listed

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