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Recruiting NCT06216002

NCT06216002 Incidence of Residual Neuromuscular Blockade in Fraility in OncoGynae Surgery

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Clinical Trial Summary
NCT ID NCT06216002
Status Recruiting
Phase
Sponsor Mahidol University
Condition Frailty
Study Type INTERVENTIONAL
Enrollment 622 participants
Start Date 2024-01-02
Primary Completion 2025-12-31

Trial Parameters

Condition Frailty
Sponsor Mahidol University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 622
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2024-01-02
Completion 2025-12-31
Interventions
Train of four nerve stimulator

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Brief Summary

Frailty among patients undergoing surgery is strongly associated with an elevated risk of adverse perioperative outcomes, heightened incidence of postoperative complications, increased mortality rates, and prolonged hospital length of stay. Our focus centers on investigating the frailty index in the context of complications experienced by patients undergoing oncologic gynecology surgery. The principal objective of this research is to elucidate the extent to which residual neuromuscular blocking agents are linked to frailty.

Eligibility Criteria

Inclusion Criteria: * Age \>,= 18 years * Patients undergoing elective gynecologic-oncology surgery Exclusion Criteria: * Unable to communicate Thai * Unable to understand the questionnaire * Preexisting neuromuscular disease * Preexisting disease involved wrist that may affect the nerve stimulator examination

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