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The effect of ASV ventilation mode on respiratory failure

Evaluation of the effect of using Adaptive support ventilation (ASV) in comparison with Synchronized intermittent mandatory ventilation (SIMV) method on lung mechanics in Respiratory Failure Patients Hospitalized in Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161106030735N2
Enrollment
64
Registered
2020-12-02
Start date
2020-11-20
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Acute hypoxemic respiratory failure. Acute respiratory failure with hypoxia

Interventions

Intervention 1: In the ASV or intervention group,Minute Volume:100% and pressure set on 30 CmH2O to reach O2Saturation: 88-92% and PEEP = 5 and flow trigger 1-3 l / min.As the patient's condition impr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 85 Years

Inclusion criteria

Inclusion criteria: Intubated patients with acute respiratory failure type I (hypoxemic) Endotracheal intubation and mechanical ventilation less than 48 hours Respiratory failure based on PaO2/FiO2=150-250 (P / F Ratio = 150-250)

Exclusion criteria

Exclusion criteria: Patients with acute respiratory failure and PaO2/FiO2( P / F Ratio) less than 150 Neuromuscular and diaphragmatic disorders Chest deformity Suspected Intracranial Hypertension Chronic obstructive pulmonary disease and severe asthma Chronic heart failure Chronic renal failure Refractory shock Diagnosed Barotrauma and Lung Contusion Age under 16 and over 85 years Pregnancy Abdominal compartment syndrome

Design outcomes

Primary

MeasureTime frame
Lung compliance. Timepoint: Measurement of lung compliance on days 1, 2, 3 and 7 after ASV or SIMV setting. Method of measurement: compliance measurment is based on ventilator information.;Lung resistance. Timepoint: Measurement of lung resistance on days 1, 2, 3 and 7 after ASV or SIMV setting. Method of measurement: resistance measurment is based on ventilator information.

Secondary

MeasureTime frame
Acute Physiologic Assessment and Chronic Health Evaluation (APACHE) II Scoring System. Timepoint: At the time of admission. Method of measurement: According to the case report.;Oxygenation based on the ratio of arterial oxygen pressure to the Fio2. Timepoint: Days 1, 2, 3 and 7 after the start of ventilation mode. Method of measurement: Based on sample information of ABG blood gas analysis.;Arterial blood carbon dioxide pressure PaCO2. Timepoint: Days 1, 2, 3 and 7 after the start of ventilation mode. Method of measurement: Based on sample information of ABG blood gas analysis.;Fentanyl intake. Timepoint: Days 1, 2, 3 and 7 after the start of ventilation mode. Method of measurement: Based on patient record (micrograms).;Number of ventilator free days at day 28. Timepoint: Twenty-eighth day after intervention. Method of measurement: Based on patient record.;Intensive care unit length of stay. Timepoint: At the time of discharge from the intensive care unit. Method of measurement: Based on patient record.;Richmond Agitation and Sedation Scale (RASS score). Timepoint: Days 1, 2, 3 and 7 after the start of ventilation mode. Method of measurement: Based on patient record.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Naseh

Tehran University of Medical Sciences

enaseh@razi.tums.ac.ir+98 21 84901

Outcome results

None listed

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