Adverse Events during Intrahospital Transport of CriticallyIll Patients
Not Applicable
- Conditions
- Health Condition 1: Z998- Dependence on other enabling machines and devices
- Registration Number
- CTRI/2024/07/070693
- Lead Sponsor
- Indira Gandhi Government Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)All critically ill patients of every age who underwent intrahospital transport are included in the study
2)All critically ill patients of either gender who underwent intrahospital transport are included in the study
Exclusion Criteria
1)Refusal to participate in study
2)patients who are not critically ill
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyse adverse events during intrahospital transport of critically illl patients and study patient outcome (survival or death ) within 24 hr .Timepoint: 1) before transport for 15 min <br/ ><br>2 During transport <br/ ><br>3) after returning to ICU for 15 min
- Secondary Outcome Measures
Name Time Method 1)To determine the nature of problems encountered during intrahospital transport. <br/ ><br>2) Preventive strategies which could be put in place to reduce observed adverse events.Timepoint: 1) before transport <br/ ><br>2 During transport <br/ ><br>3) after returning to IC