Actively Recruiting
Diagnostic Feasibility of 100 Hz Tetanic Stimulation
Led by University of Debrecen · Updated on 2025-03-27
40
Participants Needed
2
Research Sites
155 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Diagnostic Feasibility of 100 Hz Tetanic Stimulation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- ASA physical status classification 1 to 3
- Body mass index (BMI) between 18.5 and 25 (normal body weight)
- Patient is in supine position with one accessible arm
You will not qualify if you...
- Diseases impairing neuromuscular function such as myopathies or severe liver and kidney failure
- Use of drugs affecting neuromuscular function including magnesium and aminoglycosides
- Pregnancy (pregnancy tests done for women of childbearing age to exclude pregnancy)
- Breast-feeding
- Acute surgery
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Department of Anesthesiology and Intensive Care, University of Debrecen
Debrecen, Hajdú-Bihar, Hungary, 4032
Not Yet Recruiting
2
University of Debrecen Medical Center, Department of Anesthesiology and Intensive Care
Debrecen, Hungary, 4032
Actively Recruiting
Research Team
A
Adrienn Pongrácz, MD PhD
CONTACT
R
Réka Nemes, MD PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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