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A Study On Detection Of Adverse Drug Reaction Using The Trigger Tool

A Prospective Observational Study On Trigger Tool Based Detection Of Adverse Drug Reactions In A Tertiary Care Teaching Hospital - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/06/053869
Enrollment
366
Registered
2023-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

None listed

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In patients of the general medicine department and patients belonging to the age group 18 years or older with at least 24 hours of length of stay and complete medical record

Exclusion criteria

Exclusion criteria: Participants with psychiatric/ rehabilitation diagnosis will be excluded. The perinatal module, emergency department, intensive care module triggers module will be excluded

Design outcomes

Primary

MeasureTime frame
The study will analyze the feasibility of the trigger tool for the prospective detection of adverse drug reactions.Timepoint: Single Point—

Secondary

MeasureTime frame
The study will describe the association between patient- specific factors and the Adverse event.Timepoint: Single point—

Countries

India

Contacts

Public ContactDr Supriya PS

N G S M Institute of Pharmaceutical Sciences Nitte (Deemed to be University), Mangaluru

jain.pranitha10@gmail.com9483582624

Outcome results

None listed

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