Effect of subglottic suctioning in patients on ventilator on pneumonia that is due to ventilatory support
- Conditions
- Respiratory disorder, unspecified,
- Registration Number
- CTRI/2021/09/036640
- Lead Sponsor
- sir Gangaram hospital
- Brief Summary
The study is a randomized controlled interventional open labelled study conducted on patients of age 18-70 years requiring mechanical ventilation for more than 48 hours. 100 patients will be enrolled divide into two group of 50 patients each- Control group intubated with conventional endotracheal tube and test group with subglottic suction port endotracheal tube. Intervention will be subglottic suction done every 2 hourly in test group. Ventilator bundles will be applied in both the groups. Screening for ventilator associated pneumonia will be done for 28 days by NHSN PNU 1 definition. Primary outcome will be the incidence of ventilator associated pneumonia and secondary outcome will be duration of mechanical ventilation and ICU stay, Rate of microbiological positive culture in VAP patients and ICU mortality. Outcomes will be analyzed in both the groups.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 100
Requiring mechanical ventilation for more than 48 hours Without suspected or confirmed community or hospital acquired pneumonia.
Prior intubation or tracheostomy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of ventilator associated pneumonia Upto 28 days after intubation
- Secondary Outcome Measures
Name Time Method Duration of mechanical ventilation and ICU stay, Rate of microbiological positive culture in VAP patients, ICU mortality uptown 28 days after intubation
Trial Locations
- Locations (1)
Sir Ganga Ram hospital
🇮🇳Delhi, DELHI, India
Sir Ganga Ram hospital🇮🇳Delhi, DELHI, IndiaDr Priya GuptaPrincipal investigator9992996985priyagupta0905@gmail.com