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An observational cohort study on the effect of prevention-centered intensive control measures on the incidence of multidrug-resistant bacterial infection in ICU

An observational cohort study on the effect of prevention-centered intensive control measures on the incidence of multidrug-resistant bacterial infection in ICU

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123523
Enrollment
Unknown
Registered
2026-04-27
Start date
2025-06-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Multi-drug resistant bacterial infection

Interventions

Novel nosocomial infection prevention and control measures group (observation group):None
Traditional hospital infection prevention and control measures group (control group):None

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age must be 18 years or older; 2.Patients who have been admitted to the ICU for more than 48 hours; 3.Individuals with complete medical records.

Exclusion criteria

Exclusion criteria: 1. Patients who were infected or isolated with MDRO before admission to ICU; 2. Patients who had catheter retention time> 48 hours before admission to ICU; 3. Non-standard microbial specimen collection and discontinuity of inflammatory marker monitoring.

Design outcomes

Primary

MeasureTime frame
The incidence rate of MDRO infections in the ICU;

Secondary

MeasureTime frame
The incidence rate of catheter infections;Days of hospitalization;Duration of invasive catheter placement;hospitalization expenses;The duration of the use of vasoactive drugs;Site of hospital infection occurrence;Prognosis;The rate of detecti multidrug-resistant organisms (MDROs) 48 hours after admission to the ICU;

Countries

China

Contacts

Public ContactFu Yanan

Northern Jiangsu People's Hospital

1183433684@qq.com+86 18051062281

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026