study of clinical information intelligent decision support system for shock patients in ICU

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100045174

Enrollment

Unknown

Registered

2021-04-07

Start date

2021-09-01

Completion date

Unknown

Last updated

2021-11-08

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

Conditions

shock

Interventions

control group:no

experimental group:clinical information intelligent decision support system was used

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Patients with shock happened in the ICU; 2. Aged >=18 years; 3. The patient or his legal representative signed the informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Pregnant women; 2. People with mental illness; 3. Patients or their legal representatives refused to participate in the trial.

Design outcomes

Primary

Measure	Time frame
the time from happen to treatment of shock;mortality rate;	—

Countries

China

Contacts

Public ContactLin Ling

Sir Run Run Shaw Hospital

linling1@zju.edu.cn+86 13588706742

Outcome results

None listed

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