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Comparison of Intubation Conditions During Rapid Sequence Induction Obtained With Modified Time Principal Induction With a Standard Intubation Dose of Rocuronium Versus Succinylcholine

StatusRecruiting
PhasePhase 4
Started2023-09-13
View on ClinicalTrials.gov ↗
Record status
This record was last updated December 10, 2024 (before its estimated June 1, 2025 completion). Its status may not reflect the trial's current state.

Amendment history

2024-12-06
Study Status v2
Primary completion date2024-09-12→2025-06-01
Completion date2024-09-12→2025-07-01
2023-11-27
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2024-02-14→2024-09-12
Completion date2024-02-14→2024-09-12
Start dateestimated 2023-09-05→confirmed 2023-09-13
Study sitesdetails revised at 1 of 1 site
2023-08-31
Original filing
The purpose of this study is to assess and compare conditions for tracheal intubation obtained with modified time principal induction with 0.6 mg/kg rocuronium and 1 mg/kg succinylcholine. Specifically, the investigators will be evaluating ease of laryngoscopy, vocal cord view, vocal cord opening, and movement of limbs and coughing during tracheal intubation in order to assess intubation conditions, to compare efficiency and success rate of tracheal intubation between two induction agents and to determine the rate of patient awareness during induction and post-operative recall of paralysis.
Trial Details
NCT Number NCT06029049
Lead Sponsor The University of Texas Health Science Center, Houston
Conditions Anesthesia
Enrollment 152 participants
Start Date 2023-09-13
Primary Completion 2025-06-01 (estimated)
Study Completion 2025-07-01 (estimated)
Updated on ClinicalTrials.gov 2024-12-10