Quantitative Versus qUAlitative NeuromoniToring of neUroMuscular Block for Non-cardiothoracic Surgery

Recruiting now · Not applicable

Conditions studied: Neuromuscular Block, Residual

In brief

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.

Key facts

Study ID

NCT07084363

Run by

The University of Texas Health Science Center, Houston

People needed

1032

Starts

2025-09-22

Expected to finish

2026-04-01

Last updated by the study team

2025-10-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient age ≥ 18 years old;
• General anesthesia with endotracheal intubation;
• Neuromuscular block with rocuronium.

You may not qualify if…

• 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)

Where it is running

• The University of Texas Health Science Center at Houston — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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