Clinical Trial

Intubation Conditions During ERCP With Lidocaine Aerosol Plus Low-dose Cisatracurium or Conventional-dose Cisatracurium

Completed Phase 4
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Summary
This clinical study investigates the effects of lidocaine aerosol as an adjunct to low-dose cisatracurium for endotracheal intubation during ERCP (Endoscopic Retrograde Cholangiopancreatography) procedures. The aim is to assess whether lidocaine aerosol can improve the clinical conditions of intubation to a level comparable to the standard dose of cisatracurium, while reducing the amount of muscle relaxant required. The study also seeks to evaluate the impact of this approach on intubation success, extubation time, and recovery time in the operating room, ultimately improving the efficiency of the operating room. Participants will be randomly assigned to either the low-dose cisatracurium group with lidocaine aerosol or the standard-dose cisatracurium group. The primary outcome is the incidence of clinically acceptable intubation conditions, defined by the Cooper's grading system.
Protocol Amendment History 3 changes
critical Trial completed 2026-05-29
notable Primary completion pushed: 2026-04-22 -> 2026-05-22 2026-05-29
minor Completion pushed: 2026-04-24 -> 2026-05-24 2026-05-29
Trial Details
NCT Number NCT07185074
Lead Sponsor Jiangang Song
Conditions Intubation, Intratracheal
Enrollment 186 participants
Start Date 2025-01-17
Primary Completion 2026-05-22 (estimated)
Study Completion 2026-05-24 (estimated)
Updated on ClinicalTrials.gov 2026-05-28