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A study to evaluate the treatment given in the ICU for pain and occurrence of altered mental status of patients in ICU

NATIONAL (iNdian AnalgosedaTION And deLirium) : Multi-center Prospective Observational Study of Current Analgo-Sedation Practices and the incidence of delirium in Indian ICUs: INSTINCT II study (INhaled SedaTion INCriTically ill patients â??INSTINCT study Group)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/10/028375
Enrollment
2000
Registered
2020-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Health Condition 1: R00-R09- Symptoms and signs involving the circulatory and respiratory systems

Interventions

Intervention1: NA: NA Control Intervention1: NA: NA

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age > 18 years 2. Anticipated duration of ventilation > 48 hrs 3. Need for sedation for >48 hrs

Exclusion criteria

Exclusion criteria: 1. Severe Brain Injury GCS 2. Mechanical ventilation needed 3. Mechanical Ventilation initiated > 24 hrs. after ICU admission (NIV counts as Mechanical Ventilation) 4. Not expected to survive for > 24 hrs. 5. Admitted for end of life care

Design outcomes

Primary

MeasureTime frame
The incidence of delirium using the CAM-ICU scoreTimepoint: From admission till discharge/death in ICU—

Secondary

MeasureTime frame
Mean (± SD) pain score each day in the ICU, and proportion of time spent in target sedation range (RASS 0 to -2).Timepoint: From admission till discharge/death in ICU—

Countries

India

Contacts

Public ContactDr Atul Kulkarni

Tata Memorial Centre

kaivalyaak@yahoo.co.in9869077526

Outcome results

None listed

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