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Comparison of ASV and PSV mode in weaning the patient from the mechanical ventilator

Comparison of ASV and PSV mode in weaning the patient from the mechanical ventilator

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230725058923N1
Enrollment
100
Registered
2024-05-26
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

The effects of ventilator modes in Head truma patient in Icu.

Interventions

Intervention 1: : Intervention group: In this prospective study, the number of 50TBI head trauma patients admitted to the General ICU. 8 and 7 of Imam Reza Hospital who were under mechanical ventilato

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age above 18 years To have satisfaction and cooperation Patients who were mechanically ventilated for more than 24 hours with PSV levels of 8 cmH2O, PEEP =8 cmH2O, and FiO2 =40% Medical stability (arterial blood gas pH = 7.35-7.45, PaO2 =60 mmHg on FiO2 =40% and PaCO2 40 ± 5 mm Hg Absence of signs and symptoms of infection Hemodynamic stability

Exclusion criteria

Exclusion criteria: acute pulmonary or systemic infection, Hemodynamic instability Previous or current neuromuscular disease (such as myasthenia gravis and Guillain-Barré disease) Patients with obstructive pulmonary disease, asthma and COPD, etc. ARDS restrictive lung disease and...

Design outcomes

Primary

MeasureTime frame
The duration of the patient's separation from the ventilator. Timepoint: From the time of connecting the patient to the ventilator until disconnecting it. Method of measurement: Clinical condition of the patient and ventilator.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKawsar Javanmardi

Tabriz University of Medical Sciences

kawsarjavanmardi99@gmail.com+98 87 3512 1264

Outcome results

None listed

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