Actively Recruiting
Quantitative Versus qUAlitative NeuromoniToring of neUroMuscular Block for Non-cardiothoracic Surgery
Led by The University of Texas Health Science Center, Houston · Updated on 2025-10-10
1032
Participants Needed
1
Research Sites
27 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to assess the effect of quantitative block monitoring versus less expensive qualitative monitoring treatment effects on the lowest SpO2/FiO2 ratio in the PACU. The results will be incorporated into an enhanced recovery pathway for surgical patients.
CONDITIONS
Official Title
Quantitative Versus qUAlitative NeuromoniToring of neUroMuscular Block for Non-cardiothoracic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient age 218 years old
- General anesthesia with endotracheal intubation
- Neuromuscular block with rocuronium
You will not qualify if you...
- Intubation before induction of anesthesia
- Critically ill patients admitted from the ICU
- Emergency cases
- Non-intubated patients
- Patients who will not be paralyzed through the surgery (spine)
- Patients with an implanted electronic device (e.g. cardiac pacemaker)
- Patients with allergies to adhesive
- Patients with pre-existing neuromuscular disease (e.g. Myasthenia Gravis)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
M
Mehmet Turan, MD
CONTACT
M
Mohammad Khudirat
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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