Neuromuscular Blockade Intubating Conditions

Overview

About this study

The purpose of this study is to compare intubating conditions at varying levels of rocuronium-induced neuromuscular blockade.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Age ≥ 18 years old.
  • Patients willing to participate and provide an informed consent.
  • Patients undergoing elective surgical procedures that require use of NMBA agents (rocuronium) administered intraoperatively.

Exclusion Criteria:

  • Patients with disorders, such as stroke, carpal tunnel syndrome, broken wrist with nerve damage, Dupuytren contracture, or any similar wrist injury.
  • Patients with systemic neuromuscular diseases such as myasthenia gravis.
  • Patients with significant organ dysfunction that can significantly affect pharmacokinetics of neuromuscular blocking and reversal agents; i.e., severe renal impairment or end-stage liver disease.
  • Patients having surgery that would involve prepping the arm into the sterile field.
  • Patients receiving a rapid sequence induction.

Eligibility last updated 8/29/22. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Johnathan Renew, M.D.

Open for enrollment

Contact information:

Johnathan Renew M.D.

(904) 956-3328

Renew.J@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20540005

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