Skeletal Muscle Index and a Neuromuscular Blocking Agent
Relationship Between Skeletal Muscle Index in Preoperative Computed Tomography and a Neuromuscular Blocking Agent Dose Required for Maintaining Deep Neuromuscular Blockage: a Prospective Observational Study.
1 other identifier
observational
90
0 countries
N/A
Brief Summary
With the recent development of image analysis, it has become possible to measure the skeletal muscle index representing the subject's muscle mass from preoperative computed tomography (CT) images. Therefore, in this study, the investigators quantify the skeletal muscle index from preoperative CT images and analyze the correlation with the dose of neuromuscular blocking agent, rocuronium, required for maintaining deep neuromuscular blockade.
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 Dec 2024
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
First Submitted
Initial submission to the registry
December 13, 2024
CompletedFirst Posted
Study publicly available on registry
December 18, 2024
CompletedStudy Start
First participant enrolled
December 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 25, 2026
ExpectedDecember 18, 2024
December 1, 2024
1 year
December 13, 2024
December 13, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Skeletal Muscle index
Muscle amount
preoperative period
Eligibility Criteria
Patients scheduled for elective colon surgery under general anesthesia
You may qualify if:
- Those who voluntarily agreed and signed the written consent form before participating in the study
- American Society of Anesthesiologists physical class (ASA class) 1-3
- Patients scheduled for elective colon surgery under general anesthesia
- Patients undergoing abdominal computed tomography for routine preoperative preparation
You may not qualify if:
- Pregnant women
- Decreased renal function (GFR\<60mL/min/1.73m2).
- Patients taking drugs that affect deep neuromuscular blockade
- Patients with a history of neuromuscular and muscle disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Officials
- PRINCIPAL INVESTIGATOR
Insun Park, M.D./Ph.D.
assistant professor
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
December 13, 2024
First Posted
December 18, 2024
Study Start
December 25, 2024
Primary Completion
December 25, 2025
Study Completion (Estimated)
December 25, 2026
Last Updated
December 18, 2024
Record last verified: 2024-12