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Clinical Trial Summary

The hypothesis of this study is that musculoskeletal point of care ultrasonography would support the GP's decision and ultimately improve patient management. The aim of this study is to evaluate, in the context of suspected musculoskeletal abnormality, the contribution of musculoskeletal point of care ultrasonography to the general practitioner's overall decision-making strategy, defined according to the following 5 axes: diagnosis (I), therapy (II), patient orientation (III), prescription of complementary examinations (IV) and follow-up (V).


Clinical Trial Description

The study circuit takes place in a single visit. 1. The investigating physician suspects a musculoskeletal anomaly following an initial clinical examination. 2. The patient (who meets the inclusion criteria and has no non-inclusion criteria) gives consent to participate, after receiving information about the study. 3. The investigator fills in the e-CRF (appendix III), clinical examination, medical interrogation and his or her decisions according to the 5 axes, which cannot be modified, as the structure of the e-CRF planned in advance does not allow backtracking. The investigator performs the targeted musculoskeletal ultrasound with his or her personal ultrasound machine, following his or her usual operating procedure. 4. The investigator fills in the e-CRF with the results of the targeted ultrasound scan and indicates any modifications to the decision axes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06068595
Study type Interventional
Source Central Hospital, Nancy, France
Contact Boris Gass, Dr
Phone 67467111
Email boris.gass@univ-lorraine.fr
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date October 2027