Actively Recruiting
Residual Neuromuscular Block in the Post-Anesthetic Unit and Postoperative Complications
Led by Dr. Negrin University Hospital · Updated on 2025-08-24
296
Participants Needed
2
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The use of neuromuscular blockers (NMB) is essential to optimize surgical conditions, ensure patient immobility during the intervention and prevent complications derived from involuntary movements. Intraoperative monitoring of neuromuscular relaxation allows the depth of neuromuscular blockade to be accurately evaluated, guaranteeing ideal conditions for the surgical team. Residual neuromuscular blockade (RNMB) is the persistence of muscle paralysis after the administration of NMB during a surgical intervention. The appearance of RNMB poses substantial challenges in the postoperative period, as it has negative repercussions for the safety and well-being of the patient.
CONDITIONS
Official Title
Residual Neuromuscular Block in the Post-Anesthetic Unit and Postoperative Complications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient undergoing surgical intervention under general anesthesia that requires the use of neuromuscular block during the study time and that required hospital admission.
- Informed consent signature.
You will not qualify if you...
- Neuromuscular disease
- Not having received neuromuscular block during the intervention
- Admission to the outpatient surgery unit
- Admission to the postoperative intensive care unit
- Patients who signed informed consent, but postoperative data could not be collected upon arrival at the PACU.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Hospital Universitario de Gran Canaria Doctor Negrín
Las Palmas de Gran Canaria, Las Palmas, Spain, 35010
Actively Recruiting
2
Ángel Becerra
Las Palmas de Gran Canaria, Las Palmas, Spain, 35019
Actively Recruiting
Research Team
Á
Ángel Becerra Bolaños, PhD
CONTACT
A
Aurelio Rodríguez Pérez, 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
1
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