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Study of Intensive Care Units in India

Indian Intensive Care Case Mix and Practice Patterns Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01384929
Acronym
INDICAPS
Enrollment
4236
Registered
2011-06-29
Start date
2010-07-31
Completion date
2011-05-31
Last updated
2011-06-29

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

Conditions

Critical Illness

Brief summary

There is scant data on the casemix and practices in Indian intensive care units (ICUs). Most of the available data comes from single centre studies. There is a dire need to have data from Indian ICUs to reflect the vast spectrum of critical care illness, services and practices. INDICAPS planned to collect data of all patients in the ICU on one particular day, and four such days spread throughout a one-year period were selected: the second Wednesday of July and October this year, i.e. July 14 and October 13, 2010 and the second Wednesday of January and April next year, i.e. January 12 and April 13, 2011. As many ICUs all over the country as possible were asked to participate. The investigators aimed to gather information about ICUs, patients in ICUs, the types and severity of illness, monitoring and therapeutic modalities used, types of infections,mortality rates, etc.

Detailed description

The following information will be analysed: Case-mix, severity of illness, prevalence of infection, hemodynamic monitoring and therapy, mechanical ventilation practices, nutrition and outcome * Seasonal and regional variations in the above * Epidemiology and variations in antibiotic use * Patterns of microorganisms and outcome * Prevalence and outcome of specific tropical febrile illnesses, including malaria, dengue fever, leptospirosis, scrub typhus * Prevalence and outcome of toxins and poisonings * Relation of ICU and hospital organizational issues to prevalence of infection and outcome * Organisation of intensive care services * End of life - Ethical decisions

Interventions

None listed

Sponsors

Indian Society of Critical Care Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients present in the ICU July 14, 2010, October 13, 2010, January 12, 2011 and April 13, 2011

Design outcomes

Primary

MeasureTime frame
All cause mortality30-days

Secondary

MeasureTime frameDescription
ICU Length of stay30 daysStay in ICU till 30 days
Hospital length of stay30 daysStay in hospital till 30 days
Hospital survival30 daysSurvival at hospital discharge or at 30 days

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026