Skip to content

Second Survey of Intensive Care in India

Indian Intensive Care Case Mix and Practice Patterns Study - II

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03631927
Acronym
INDICAPS-II
Enrollment
5094
Registered
2018-08-15
Start date
2018-08-23
Completion date
2019-05-11
Last updated
2021-11-11

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

Conditions

Critical Illness

Keywords

critical care unit

Brief summary

INDICAPS was the first large scale, multicentre survey launched by the ISCCM. The aim was to gather information about ICUs, organizational characteristics, patient casemix, the types and severity of illness, monitoring and therapeutic modalities used, types of infections, and other such data. This was performed between July 2010 and April 2011 and published in 2016.\[1\] Over the last 8 years, there has been a significant difference in the delivery of intensive care services, critical care education, socioeconomic indicators, antibiotic resistance patterns and other aspects of practices in Indian ICUs. It is therefore necessary to revisit and resurvey the current trends in intensive care practices in India, and to reflect the vast spectrum of critical care illness, services and practices. Similar to INDICAPS, which was a point-prevalence study of all patients present in the ICU on four different days over a one-year period, INDICAPS II will record data of all patients admitted to the ICU on 4 different days.

Detailed description

INDICAPS II will record data of all patients admitted to the ICU on 4 different days (August 23, 2018; October 25, 2018; December 13, 2018; April 11, 2019) in a cross-sectional design. Data collection includes: 1. On admission: demographic characteristics, comorbidities, source of admission, primary and secondary admission diagnoses, 2. Baseline data (on the study day), including parameters used to calculate SAPS II score and SOFA score and infections, 3. Information on monitoring modalities, mechanical ventilation, nutrition, fluid therapy, other routine ICU practices c. Outcome at ICU and hospital discharge d. Organisation of ICU services

Interventions

OTHERObservation

Observation

Sponsors

Indian Society of Critical Care Medicine
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients present in the ICU on August 23, 2018; October 25, 2018; December 13, 2018; April 11, 2019

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
ICU Mortality30 days from the study dayNumber of patients who died in the ICU, as well as those terminally discharged from the ICU

Secondary

MeasureTime frameDescription
Hospital Mortality30 days from the study dayall cause hospital mortality, including those terminally discharged from the ICU
ICU Length of Stayupto 30 days from the study daylength of stay in the intensive care unit
Hospital Length of Stayupto 30 days from the study daylength of stay in the hospital

Countries

India

Participant flow

Participants by arm

ArmCount
Single Cohort
All patients \> 15 years of age present in the intensive care unit on the study days
4,669
Total4,669

Baseline characteristics

CharacteristicSingle Cohort
Age > 15 years4669 Participants
Age, Continuous56.9 years
STANDARD_DEVIATION 17.4
Ethnicity (NIH/OMB)
Asian (Indian) ethnicity 4669
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Asian (Indian) ethnicity 4669
Not Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Asian (Indian) ethnicity 4669
Unknown or Not Reported
4669 Participants
Region of Enrollment
India
4669 participants
Sex: Female, Male
Female
1696 Participants
Sex: Female, Male
Male
2973 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
1,164 / 4,669
other
Total, other adverse events
0 / 4,669
serious
Total, serious adverse events
0 / 4,669

Outcome results

Primary

ICU Mortality

Number of patients who died in the ICU, as well as those terminally discharged from the ICU

Time frame: 30 days from the study day

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Single CohortICU Mortality1092 Participants
Secondary

Hospital Length of Stay

length of stay in the hospital

Time frame: upto 30 days from the study day

ArmMeasureValue (MEDIAN)
Single CohortHospital Length of Stay12 Days
Secondary

Hospital Mortality

all cause hospital mortality, including those terminally discharged from the ICU

Time frame: 30 days from the study day

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Single CohortHospital Mortality1164 Participants
Secondary

ICU Length of Stay

length of stay in the intensive care unit

Time frame: upto 30 days from the study day

ArmMeasureValue (MEDIAN)
Single CohortICU Length of Stay6 days

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026