FindTrial
Sign In

The impact of integrated clinical information system(ICIS) implementation in the ICU upon the quality of care.

The impact of integrated clinical information system(ICIS) implementation in the ICU upon the quality of care.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16008555
Enrollment
Unknown
Registered
2016-05-29
Start date
2016-06-01
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

Critically ill patients

Interventions

1)Control group:before the implementation of ICIS (BEFORE) and 2) Experimental group: after implementation of ICIS (AFTER):Implementation of integrated clinical information system(ICIS)

Sponsors

Zhoupu Hospital Affiliated to Shanghai University of Medicine & Health Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Admitted to our hospital ICU patients.

Exclusion criteria

Exclusion criteria: 1. Aged less than 18 years old; 2. died within 24 hours.

Design outcomes

Primary

MeasureTime frame
Standardized Mortality Ratio;—

Secondary

MeasureTime frame
The rate of unplanned decannulation (UD) in Intensive Care Unit;The incidence of ventilator associated pneumonia (VAP) in Intensive Care Unit;The incidence of intravascular catheter-related bloodstream infection (CRBSI) in Intensive Care Unit;The incidence of catheter associated urinary tract infection (CAUTI) in Intensive Care Unit;The rate of compliance with 3-hour sepsis bundles in patients with Septic shock;The rate of compliance with 6-hour sepsis bundles in patients with Septic shock;—

Countries

China

Contacts

Public ContactQiu Zeliang

Zhoupu Hospital Affiliated to Shanghai University of Medicine & Health Sciences

zlqiu1121@163.com+86 18121216112

Outcome results

None listed

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