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Adverse Events during Intrahospital Transport of Critically Ill Patients

To study the incidence of adverse events during intrahospital transport of critically ill patients A prospective observational study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/07/070693
Enrollment
100
Registered
2024-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: Z998- Dependence on other enabling machines and devices

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Indira Gandhi Government Medical College
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: 1)Refusal to participate in study 2)patients who are not critically ill

Design outcomes

Primary

MeasureTime frame
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 2 During transport 3) after returning to ICU for 15 min—

Secondary

MeasureTime frame
1)To determine the nature of problems encountered during intrahospital transport. 2) Preventive strategies which could be put in place to reduce observed adverse events.Timepoint: 1) before transport 2 During transport 3) after returning to ICU—

Countries

India

Contacts

Public ContactDr Ajay Sood

Indira Gandhi Government Medical College , shimla

ajay_5644@yahoo.com9418028130

Outcome results

None listed

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