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Review the effect of using Persian Weaning Tool in the weaning of head trauma patients from mechanical ventilation .

Assessing the effect of using Persian Weaning Tool in the weaning of head trauma patients from mechanical ventilation in Shahid Rajai Hospital in Qazvin.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171212037848N1
Enrollment
60
Registered
2018-04-27
Start date
2018-02-19
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Patients under mechanical ventilation.

Interventions

Intervention 1: The "intervention group" in this group of patients who have entry criteria are scored by the Parsian Separation Scale. If a score of 57 is reached, the candidate patient is separated a

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with head injuries Having at least 18 years of age. Not having heart disease - chronic pulmonary disease. GCS above 9

Exclusion criteria

Exclusion criteria: Exit tracheal spontaneously Unsuccessful weaning history Transferring the patient to other parts. Surgery during the study

Design outcomes

Primary

MeasureTime frame
Reduce the duration of mechanical ventilation use. Timepoint: After 48 hours of intubation. Method of measurement: The number of days that patients are under mechanical ventilation.;The Effect of Using Persian weaning Tool on Improving Quality of Care in Patients in Intensive Care Units. Timepoint: After 48 hours of intubation. Method of measurement: Comparison of complications in ICU in both control and intervention groups.;Reduce mortality in patients under mechanical ventilation. Timepoint: Until the discharge from the Intensive Care Units. Method of measurement: Comparison of mortality rate in the intervention and control groups until discharge from the intensive care unit.;Reduction of mechanical ventilation complications in patients. Timepoint: After 48 hours of intubation. Method of measurement: Comparison of the incidence of complications of mechanical ventilation in the control and intervention groups.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSareh Mohammadi

Qazvin University of Medical Sciences

s.mohammadi@qms.ac.ir+98 28 3333 6001

Outcome results

None listed

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