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Clinical Trials/NCT07312019
NCT07312019
Not yet recruiting
Not Applicable

Optimization of Medical Time in the Emergency Department: Impact of an AI-Based System on Prescription Entry

Centre Hospitalier Universitaire, Amiens1 site in 1 country770 target enrollmentStarted: January 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
770
Locations
1
Primary Endpoint
Medical time required for the transcription of prescriptions

Overview

Brief Summary

Drug-related iatrogenesis is a major public health issue, accounting for a significant proportion of adverse events and hospitalizations in emergency departments. Optimizing prescription management in this context is critical to improve both patient safety and physician efficiency This study aims to evaluate the impact of the POSOS AI-driven device on the medical time required for prescription management in polymedicated patients admitted to emergency departments. The main objective is to establish whether the use of POSOS can reduce transcription time compared to standard electronic management.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age ≥18 years
  • Admission to emergency department at a participating center
  • Polymedicated patients with prescriptions including ≥8 medication lines (including those for long-term illnesses)
  • Signed informed consent

Exclusion Criteria

  • Patient under legal protection/judicial measures (guardianship/custody)
  • Lack of signed informed consent

Outcomes

Primary Outcomes

Medical time required for the transcription of prescriptions

Time Frame: Day 1

Medical time required for the transcription of prescriptions for at-risk polymedicated patients at emergency admission. This is measured by the duration needed to transcribe prescriptions into the structured electronic health record by physicians, assessed by direct observation with a stopwatch

Secondary Outcomes

  • Number of drug-related problems (DRPs) identified per patient(day 1)
  • Identification of DRPs by subtype and severity(day 1)
  • Rate of reconciled medication histories and structured documentation(day 1)
  • Proportion and type of transcription errors (medication name or dosage)(day 1)
  • Readmission rates(at 3 months)
  • Mapping of DRPs by subtype and severity(day 1)
  • Time delays between triage, anamnesis, and diagnosis(day 1)
  • Length of emergency department stay and downstream hospitalizations(day 1)
  • Overall survival(at 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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