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Effect of mechanical ventilation on hemodynamic

Effect of Airway Pressure Release Ventilation on patient' hemodynamic after Coronary Artery Bypass Graft

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013092414756N1
Enrollment
32
Registered
2015-01-17
Start date
2014-11-07
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

Coronary artery disease. Atherosclerotic heart disease

Interventions

Intervention 1: Intervention of this research is a ventilation mode is called Airway Pressure Release Ventilation that applied through ventilator and tracheal tube for half an hour. this mode is a inv
Intervention of this research is a ventilation mode is called Airway Pressure Release Ventilation that applied through ventilator and tracheal tube for half an hour. this mode is a inverse ratio mode
This study is a cross-over study and no control group. Intervention (APRV mode) compared with SIMV mode. synchronized intermittent mandatory ventilation is a usual mode of mechanical ventilation in re

Sponsors

Mashhad University of Medical Sciencse- research assisstance
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 40-70 years old; hemodynamic stability in the first visit; EF = 40% ; RASS = -2 to -3; surgery OFF PUMP; CABG without repair or replace the valve; failure to perform CPR during surgery or before the study; failure to perform emergency surgery (out of routine preoperative); absence of underlying lung disease; lack of oxygenation and ventilation disorder; having hypertension before surgery. Exclusion criteria: CPR performed during study; the need to replace volume; -2< RASS <-3; bleeding more than 100ml / hr of Drains; need to have surgery again; pH arterial <7.25; dysrhythmia that lead to the development of hemodynamic changes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cardiac index. Timepoint: before intervention, half an hour after intervention & half an hour after return to base mode. Method of measurement: lit/min/BSA.;Stroke volume index. Timepoint: before intervention, half an hour after intervention & half an hour after return to base mode. Method of measurement: mi/BSA.;Mean arterial pressure. Timepoint: before intervention, half an hour after intervention & half an hour after return to base mode. Method of measurement: mmHg.;Systemic vascular resistance. Timepoint: before intervention, half an hour after intervention & half an hour after return to base mode. Method of measurement: Dynes?/?sec?/?cm5?.

Secondary

MeasureTime frame
Arterial oxygen saturation. Timepoint: before intervention, half an hour after intervention & half an hour after return to basic mode. Method of measurement: percent.;Ratio ofl arterial oxygen to inspired oxygen fraction. Timepoint: before intervention, half an hour after intervention & half an hour after return to basic mode. Method of measurement: number.;Pressure of arterial co2. Timepoint: before intervention, half an hour after intervention & half an hour after return to basic mode. Method of measurement: mmHg.;Pressure of arterial oxygen. Timepoint: before intervention, half an hour after intervention & half an hour after return to basic mode. Method of measurement: mmHg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Malekzadeh

Mashhad University of Medical Sciences

malekzadehj@mums.ac.ir+98 51 3859 5511

Outcome results

None listed

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