The Association Between Residual Neuromuscular Block Risk Prediction Score and the Train-of-Four Ratio
Residual Paralysis in the Post Anesthesia Care Unit: The Association Between Residual Neuromuscular Block Risk Prediction Score and the Train-of-Four Ratio. A Prospective Single-Center Open-Label Cohort Study
1 other identifier
observational
91
1 country
1
Brief Summary
evaluate the degree of association, and the predictive accuracy of the REPS (as a predictive tool) compared with the TOFr as a quantitative assessment tool for (rNMB) in surgical patients in the early postoperative phase. The TOFr will be measured at 0, 15, 30, 45, and 60 min after extubation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2024
CompletedFirst Submitted
Initial submission to the registry
March 21, 2025
CompletedFirst Posted
Study publicly available on registry
March 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedMarch 27, 2025
October 1, 2024
1.2 years
March 21, 2025
March 26, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
correlation between residual neuromuscular block risk prediction score and train of four
1 hour
Interventions
it is a clinical tool designed to estimate the likelihood of residual neuromuxcular blockade in postoperative patients
Eligibility Criteria
Patients who will be scheduled to undergo elective surgical procedures requiring the use of neuromuscular blocking drugs.
You may qualify if:
- Age group 18-65 years old
- Both genders
- Patients with American Society of Anesthesiologist physical status classification of 1 or 2.
You may not qualify if:
- Patients who are less than 18 years old or more than 65 years old.
- Patients with planned scheduled recovery in the intensive care unit or if more than 10 minutes had elapsed since tracheal extubation until NMB monitoring at the PACU.
- Patients on medications that interfere with muscle activity.
- Known allergy to neuromuscular blocking agents.
- Pregnancy or suspected pregnancy.
- Neuro-muscular diseases.
- Patients refusing to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Assiut University Hospitals
Asyut, 71111, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
March 21, 2025
First Posted
March 27, 2025
Study Start
August 1, 2024
Primary Completion
October 1, 2025
Study Completion
April 1, 2026
Last Updated
March 27, 2025
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share