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N/A N=655

Point of Care Ultrasound Use by General Practitioners in France (Echo-MG)

Point of Care Ultrasound

Enrolled (actual)
655
Serious AEs
Results posted
Jan 2026
Primary outcome: Primary: Number of Patients With Change in the Diagnosis After POCUS Examination — 397 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Sorbonne University
Primary completion
Jul 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients With Change in the Diagnosis After POCUS Examination
397
PRIMARY
Number of Patients With Change in Diagnostic Confidence
552
PRIMARY
Number of Patients With Change in the Referral Plan
363
PRIMARY
Number of Patients With Change in the Planned Treatment
215

Summary

This study explores how Point of Care Ultrasound (POC-US) is used in general practice in France and how it affects the diagnostic process and treatment of patients. General practitioners (GPs) will register information each time they use POC-US during a one month period. The aim of this study is to describe the use of POCUS and its role in the diagnostic and therapeutic process in general medicine. * Description of the use of POCUS through indication, organs scanned, findings, frequency , time consumption. * Analysis of the role of POCUS in the diagnostic process: change of diagnostic hypotheses and change of certainty in the main diagnostic hypothesis. * Analysis of the role of POCUS in the therapeutic process: change in the care pathway and the therapeutic initial plan. This is an observational study without any intervention.

Eligibility Criteria

Inclusion Criteria

  • minimum use of POCUS on two anatomical areas
  • GP activity for minimum two days / week
  • A minimum of two scanning probes
  • Previous participation in formal education in the use of POC-US
  • Minimum six-month experience with POCUS in general practice.
  • Estimated use of POCUS on a daily basis (average)

Exclusion Criteria

  • Conflict of interest, e.g. if the GP is part of the research group or if the GP has/had direct financial interest in selling ultrasound devices.
  • If less than five patients have been enrolled
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04583670). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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