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To study the pattern of routine instillation of medication in respiratory system in critically ill patients

Not Applicable
Completed
Conditions
Health Condition 1: J99- Respiratory disorders in diseasesclassified elsewhere
Registration Number
CTRI/2022/09/045679
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
218
Inclusion Criteria

During a study period of four weeks, all newly admitted adult patients in participating ICU will be considered for inclusion in the study if they meet any one of the below criteria

1. Patients having artificial airways with or without the need for mechanical ventilation

2. Patients requiring non-invasive ventilation

Exclusion Criteria

AGE <18 YEARS

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
(a)Types of drugs delivered as aerosol therapy and their dose and frequency <br/ ><br>(b)Method of aerosol drug delivery in ICU patients <br/ ><br>Timepoint: 4 WEEKS
Secondary Outcome Measures
NameTimeMethod
(a)Types of drugs and their doses and frequency used in ICU patients having acute respiratory distress syndrome (ARDS) <br/ ><br>(b)Method of aerosol drug delivery in ICU patients having acute respiratory distress syndrome (ARDS) <br/ ><br>Timepoint: 4 WEEKS
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