Diagnostic Feasibility of 100 Hz Tetanic Stimulation
ConditionPolyneuropathies
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorUniversity of Debrecen
About this trial
The goal of this observational study is to investigate the applicability of 100 Hz tetanic stimulation with an electromyography device in the exclusion of postoperative residual neuromuscular block. The aim is to determine whether fatigue develops with 100 Hz tetanic stimulation in anaesthetized, non-relaxed patients with normal or abnormal baseline electroneurographic (ENG) findings.
Eligibility criteria
Qualifiers
ASA 1-3;
BMI 18.5-25 (normal body weight);
patient is in supine position with one arm accessible.
Disqualifiers
diseases with impaired neuromuscular function (myopathies, severe liver and kidney failure);
drugs affecting neuromuscular function (magnesium, aminoglycosides);
pregnancy (pregnancy tests are carried out in women of childbearing age to rule out pregnancy);
breast-feeding;
Trial design
Treatments tested in this trial
- Not listed
Trial groups
40 Participants
are grouped into 2 trial groupsSponsors and collaborators
Source ClinicalTrials.gov