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The effect of using critical care service team on mortality of acutely ill patients

The effect of using critical care service team in comparison to routine care on mortality of acutely ill patients in general wards

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107187053N1
Enrollment
Unknown
Registered
2015-07-07
Start date
2010-07-17
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Acutely Ill Patients.

Interventions

Intervention 1: The intervention group: In this study the intervention group will receive the critical care service (CCS). The steps of intervention will be training of ward nurses, admitting acutly
b) patients will discharge from ICU
and c) the CCS team can actively identify patients in the wards. Ward nurses will identify patients requiring intervention by the CCS based on the standard criteria. The ward nursing staff will report
they will inform the CCS team. Then the CCS team will attend the patient’s bedside. The patient’s care is taken over by the CCS team if the patient has a acute condition. If the patient is assess and
Treatment - Other
The intervention group: In this study the intervention group will receive the critical care service (CCS). The steps of intervention will be training of ward nurses, admitting acutly ill patients (AI
and c) the CCS team can actively identify patients in the wards. Ward nurses will identify patients r
Control group: This group will recieve routine ward care and usual practices vis-a-vis urgent patient situaions

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The role of CCS is to deliver care in the non-critical care units of general hospital wards and all patients who will admit to these wards were included in the trial. Exclusion criteria are burn;cardiac surgery; pediatric and neonatal patients .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Number of deaths. Timepoint: during three phases of recieving routtine care, while on training and while recieving intervention. Method of measurement: Physician’s certification of death.;Number of Cardio-pulmonary resucitations. Timepoint: during three phases of recieving routtine care, while on training and while recieving intervention. Method of measurement: A CPR call that was made for the patient (was called code 145 in study setting) and completed CPR forms in the medical records of the patient.

Secondary

MeasureTime frame
Length of stay. Timepoint: during three phases of recieving routtine care, while on training and while recieving intervention. Method of measurement: Total days of patients hospitalization according to the hospital information system.;Admission to ICU. Timepoint: during three phases of recieving routtine care, while on training and while recieving intervention. Method of measurement: Number of patient who will admit to the ICU from general wards (medical and surgical).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Jeddian

Tehran University of Medical sciences

jeddian@mohme.gov.ir+98 21 8490 2101

Outcome results

None listed

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