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Evaluation of Ultra-portable Ultrasound in General Practice

Pragmatic Evaluation of Ultra-portable Ultrasound for a List of Indications in General Practice

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04127149
Acronym
EPEMedG
Enrollment
166
Registered
2019-10-15
Start date
2019-12-03
Completion date
2021-10-20
Last updated
2025-12-19

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

Conditions

Fracture of Long Bones, Hepatic Colic or Cholecystitis, Intra-uterine Pregnancy or Extra-uterine Pregnancy or Miscarriage, Phlebitis, Pleural Effusion, Pneumonia, Renal Colic, Subcutaneous Abscess or Cyst

Keywords

ultrasound scanner, sonogram, general practice

Brief summary

This is an interventional multi-centre study comparing two groups of general practitioners with or without an ultrasound scanner over a period of 6 months. The evaluation focuses on the management of patients for 8 pathologies: * Pneumonia * Pleural effusion * Renal colic * Hepatic colic or cholecystitis * Subcutaneous abscess or cyst * Fracture of long bones * Intra-uterine pregnancy or extra-uterine pregnancy or miscarriage * Phlebitis The principal hypothesis is that there are fewer complementary exams in the group of doctors using ultrasound scanners. The secondary hypotheses are: * There is better patient orientation (emergency care, specialist consultation, return home) in the group of doctors using the ultrasound scanners. * The global cost of the care is lower in the group of doctors using the ultrasound. * Using ultrasound during the consultation decreases the anxiety of the patient. * Using ultrasound increases the duration of the consultation. * There is no difference between the predicted and the real orientation of the patients.

Interventions

DIAGNOSTIC_TESTUltrasound scan

The group uses an ultrasound device for the consultation.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients age 18 and over * consulting their general practitioner for one of the 8 conditions below

Exclusion criteria

* patients who have already received an imagery exam for the acute episode justifying the consult * opposition to participate

Design outcomes

Primary

MeasureTime frameDescription
Number of complementary examsTwo weeks after inclusionTwo weeks after the initial consultation, with or without ultrasound scanners, the general practitioners call their patients to know: * The number of imagery exams they had (ultrasound, MRI, scanner, radiology…) * The number of biological analysis (CRP, ASAT, ALAT, Lipase…)

Secondary

MeasureTime frameDescription
Number of hospitalisations, specialist orientation or return homeTwo weeks after inclusionTwo weeks after the initial consultation, with or without ultrasound scanners, the general practitioners call their patients to know if within the past two weeks, they have been hospitalised, required emergency care, needed to consult a specialist, or returned back home
Cost of careFour weeks after inclusion in the studyAfter knowing the patient orientation and the complementary exams they had, an estimation of the cost of care is made.
Anxiety score measured by the State-Trait Anxiety Inventory (STAI-Y) scaleTwo weeks after inclusion in the studyTwo weeks after the initial consultation, with or without ultrasound scanners, the general practitioners call their patients to know the result of the anxiety test they took the day of the first consultation.
Consultation durationTwo weeks after inclusion in the studyThe day of the first consultation, the general practitioner writes the time spent

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026