FindTrial
Sign In

To see the effectiveness of ETT with Subglottic suction device in prevention of VAP over conventional ET tube

Intermittent subglottic suction for prevention of Ventilator associated pneumonia in emergency medical patients-an open label parallel group randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050983
Enrollment
60
Registered
2023-03-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: J00-J99- Diseases of the respiratory system

Interventions

Intervention1: intermitent subglottic suction : We plan to conduct a study with a group of patients receiving intermittent subglottic suction every 4-6 hours with standard ET care vs group receiving s

Sponsors

Post graduate institute of medical education and research chandigarh
Lead Sponsor
Dr pallvi
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Neurological symptoms CVS symptoms sepsis and MODS Poisoning patients Snake venum patients

Exclusion criteria

Exclusion criteria: 1. community acquired pneumonia 2. Hospital acquired pneumonia 3. ARDS 4. Immunocompromised hosts 5. Trauma patients 6. Pregnant females 7. Surgical patients 8. COVID positive patients 9. Intubated outside PGIMER

Design outcomes

Primary

MeasureTime frame
Incidence of VAPTimepoint: 14days—

Secondary

MeasureTime frame
Secondary VAP Length of stay Duration of ventilationTimepoint: 14 days—

Countries

India

Contacts

Public ContactDr Saurabh c sharda

PGIMER Chandigarh

saurabhcsharda@gmail.com9868404808

Outcome results

None listed

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