Skip to content

comparison of Adaptive Support Ventilation (ASV) and Synchronized Intermittent Mandatory Ventilation (SIMV) modes

The comparison of respiratory parameters in mechanical ventilation with Adaptive Support Ventilation (ASV) and Synchronized Intermittent Mandatory Ventilation (SIMV) in the hospitalized neurosurgical patients in ICU

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015112016151N3
Enrollment
54
Registered
2015-11-28
Start date
2015-08-23
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

mechanical ventilation. Other specified medical care

Interventions

Intervention 1: Intervention group 1: sedation will be done for patients (with propofol 1-2 mg/kg/h) if they need. Patients will be given 1 mg midazolam (bolus) if they can’t tolerate the tracheal tub
Treatment - Devices
Intervention group 1: sedation will be done for patients (with propofol 1-2 mg/kg/h) if they need. Patients will be given 1 mg midazolam (bolus) if they can’t tolerate the tracheal tube (to be in Rams
Intervention group 2: sedation will be done for patients (with propofol 1-2 mg/kg/h) if they need. Patients will be given 1 mg midazolam (bolus) if they can’t tolerate the tracheal tube (to be in Rams

Sponsors

Vice chancellor of research of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: hospitalized in neurosurgery ICU; decreased consciousness; need to intubation and mechanical ventilation; no respiratory failure. Exclusion criteria: severe liver failure (ascites, abnormal liver function tests); severe liver and renal failure ; severe lung disease based on PFT (FEV130); pregnancy; smoking; respiratory failure (MAP38, PH50, PO2<60 with FiO2<0.6); involvement or lesion of brain stem.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Peak airway pressure. Timepoint: minutes 10,20,30. Method of measurement: cm H2O by ventilator.;Static lung compliance. Timepoint: 30 minutes after intervention. Method of measurement: ml/cm H20 by ventilator.;Dynamic lung compliance. Timepoint: 30 minutes after intervention. Method of measurement: ml/cm H20 by ventilator.

Secondary

MeasureTime frame
Arterial CO2. Timepoint: minutes 10,20,30. Method of measurement: mmHg by ABG.;Arterial oxygen presuure. Timepoint: minutes 10,20,30. Method of measurement: mmHg by ABG.;Respiratory rate. Timepoint: minutes 10,20,30. Method of measurement: rate in minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Pournajafian

Iran University of Medical Sciences

alipn78@yahoo.com; pournajafian.ar@iums.ac.ir+98 21 8894 6762

Outcome results

None listed

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