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Effect of mechanical ventilation on oxynation and hemodynamic in head trauma.

The Effect Comparison of synchronized intermittent mandatory ventilation and airway pressure release ventilation in oxynation and hemodynamic parameters in patients with head trauma.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016080729234N1
Enrollment
72
Registered
2017-06-06
Start date
2016-08-22
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

Head trauma. Other intracranial injuries, Intracranial injury with prolonged coma,Traumatic subarachnoid haemorrhage,Traumatic subdural haemorrhage,Diffuse brain injury,Focal brain injury,Epidural haemorrhage,

Interventions

Intervention 1: Intervention of this research is a ventilation mode is called Airway Pressure Release Ventilation that will be applied through ventilator and tracheal tube for half an hour. This mode
Intervention of this research is a ventilation mode is called Airway Pressure Release Ventilation that will be applied through ventilator and tracheal tube for half an hour. This mode is an inverse ra
The patients in group 2 will receive APRV for two hours and after that ABG will be taken half an hour and two hours after changes. Then ventilator mode will be switched to SIMV for two hours and ABG w

Sponsors

Vice Chancellor for research of Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 15 and 60 years; patients suffering from traumatic brain injuries who are intubated and are under mechanical ventilation with SIMV mode; stable hemodynamic (MAP more than 70 mm Hg for at least 30 minutes before the start of the study); Glasgow Coma Scale <9 ; no history of chronic obstructive pulmonary disease (COPD); Exclusion criteria: unstable hemodynamic (MAP <70); need to CPR.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pressure of arterial oxygen. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Atrial blood gas (ABG).;Pressure of arterial CO2. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Atrial blood gas (ABG).;Aterial oxygen saturation. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Monitore.

Secondary

MeasureTime frame
Mean artery pressure. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Sphygmomanometer.;Heart rate. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Number in minute.;Systolic pressure. Timepoint: Before intervention, half an hour and 2 hours after intervention. Method of measurement: Sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Khalili

Sabzevar University of Medical Sciences

khalili894@gmail.com+98 51 4401 1300

Outcome results

None listed

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