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

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

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with direct acting anticoagulant adverse reaction, emg, and other related conditions. The study is currently recruiting participants at 2 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(2)

University Hospital Brno

Brno, Czech Republic, Czechia

University hospital Brno

Brno, Czech Republic, Czechia

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NCT07166302


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