RecruitingNCT07166302

Ultrasound Evaluation of Hematoma Risk After Needle EMG in Patient on DOAC Therapy

Sponsor

Masaryk University

Enrollment

70 participants

Start Date

Sep 1, 2025

Study Type

OBSERVATIONAL

Conditions

Neuromuscular Diseases (NMD)Polyneuropathies Peripheral Neuropathies Mononeuropathies EMG Direct Acting Anticoagulant Adverse Reaction Needle Injury

Summary

Approximately 30 minutes after needle EMG, patients who are taking direct oral anticoagulants (DOACs) will undergo an ultrasound examination to evaluate for the presence of possible intramuscular hematomas at the muscles where the EMG needle was inserted. These hematomas are considered a potential adverse effect of needle EMG. The aim of the study is to determine whether needle EMG can be considered a safe procedure in this group of patients, without posing a risk of intramuscular hematoma formation.

Eligibility

Inclusion Criteria4

Subjects must understand the nature of the study and must provide signed and dated written informed consent prior to conducting any study-related procedures
Willing and able to comply with all protocol procedures
subjects confirmed the daily (and recent) intake od direct anticoagulants in strandard dosing.
no other antitrombotic drug therapy (e.g. acetylsalicyl acid, clopidogrel, ticagralol, low molecular weight heparin or second direct anticoagulant) is taken.

Exclusion Criteria2

Any clinically significant medical or psychiatric condition or medical history that, in the opinion of the investigator, would interfere with the subject's ability to participate in the study or increase the risk of participation for that subject
other antitrombotic drug therapy (e.g. acetylsalicyl acid, clopidogrel, ticagralol, low molecular weight heparin or second direct anticoagulant) is recently taken.

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