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Effect of giving antibiotic into the lungs in patients with lung infection on ventilator

Effect of endobronchial administration of Colistin on outcomes in patients with Ventilator Associated Pneumonia: a randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093651
Enrollment
80
Registered
2025-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: J15- Bacterial pneumonia, not elsewhereclassified

Interventions

Intervention1: Group BI (Both Bronchoscopic instillation and Intravenous antibiotic group): Group BI (Both Bronchoscopic instillation and Intravenous antibiotic group) will receive the prescribed dose

Sponsors

ALL INDIA INSTITUTE OF MEDICAL SCIENCES,RISHIKESH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients both male and female aged more than 18 years 2.Diagnosed as ventilator associated pneumonia with a CPIS score of more than 6 3.Culture positive for organisms with intermediate sensitivity to Colistin 4. Intubated on Ventilator support

Exclusion criteria

Exclusion criteria: 1.Patients/next of Kin refusal to consent. 2.Patients with Multiple Organ Dysfunction Syndrome (MODS),septic shock at the beginning of the study. 3.Patients with a P/F (PaO2/FiO2) ratio below 100 4.Patients with severe COPD more than Grade GOLD 3E 5.Patients with recent myocardial infarction within 6 months or Heart failure with reduced Ejection Fraction (HFrEF) with Ejection Fraction (EF) less than 40 percentage 6.Immunodeficient patients 7.History of allergy to Colistin 8.Patients with infections resistant to Colistin

Design outcomes

Primary

MeasureTime frame
To compare ventilator free daysTimepoint: till day 28

Secondary

MeasureTime frame
CPIS scoreTimepoint: Day 7;CPIS score less than 6Timepoint: till day 7;To compare the mortality between the two groupsTimepoint: within 28 days;To compare the length of ICU-stay between the two groupsTimepoint: till day 28;To compare the length of hospital-stay between the two groupsTimepoint: till day 28;adverse effectsTimepoint: till 3 days

Countries

India

Contacts

Public ContactDr Deepak Singla

AIIMS RISHIKESH

deepak10.4u@gmail.com9068504999

Outcome results

None listed

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