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Study to evaluate how trigger tools help identify adverse drug events in patients admitted to the Emergency Intensive Care Unit

Performance of Trigger Tools in Identifying Adverse Drug Events in Emergency Intensive Care Unit: A Prospective Observational Study. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/07/113821
Enrollment
350
Registered
2026-07-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention1: Nil: Nil

Sponsors

Sri Ramachandra Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 years and above Patients admitted to the Intensive Care Unit ICU during the study period

Exclusion criteria

Exclusion criteria: Patients admitted to the ICU for less than 24 hours Patients with incomplete or missing medical records that prevent trigger tool assessment

Design outcomes

Primary

MeasureTime frame
To determine the effectiveness of trigger tools in detecting ADEs in ICU patientsTimepoint: 4 weeks—

Secondary

MeasureTime frame
To categorize identified ADEs based on severity preventability and causalityTimepoint: 4 weeks—

Countries

India

Contacts

Public ContactDr.A. Sumanth Reddy

Sri Ramachandra Institute of Higher Education and Research

sumathreddy.28@gamil.com9789913063

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026