patients under mechanical ventilation.
Conditions
Interventions
on every patients two intervention was performed with a 3 hours interval. we divided patients randomaly in to two group. on patient in group A in first phase of study endotracheal suctioning was pe
Treatment - Other
Sponsors
Zanjan University of Medical Sciences and Health Services
Eligibility
Sex/Gender
Male
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: men patients with stable hemodynamic status within 18-70 years old, wiht Hct more than 25%, without hyperthermia, chest injury, chst tube, chest surgery and ventilated on PEEP mode, patient with active asthma and emphysema, using endotracheal suctioning 1 hours before intervention. Exclusion criteria: reciving any kind of parlytic mascular drug like Pavlon in invention time zone, start/stop or chnage in vasodilator drug in invention time zone, change in ventilator setup, using endotracheal suctioning 1 hours before each phase of intervention, changing ventilator mode as with CMV mode.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Arterial blood oxygenation. Timepoint: 5 minutes befor and 15 and 25 minutes after intervention in each phase. Method of measurement: using vital sign monitoring system with Poyandegan Rahe Saadat made in Iran. | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital sign including Blood pressure, pulse, respiratory rate. Timepoint: 5 minutes before and 15 and 25 after intervention in each phase. Method of measurement: mm/hg for BP, number for Pulse and respiratory rate announced by vital sign monitoring system Pooyandegan rahe Saadat made by Iran. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMitra payami Bousari
Zanjan University of Medical Sciences and Health Services
Outcome results
None listed