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NCT05294523

Rocuronium and Supramaximal Stimulation

Status unknown NA Last updated 29 November 2022
What this trial tests

NA trial testing Rocuronium priming dose in Neuromuscular Blockade in 300 participants. Status unknown.

Timeline
20 December 2021
Primary endpoint
31 December 2024
31 December 2024

Quick facts

Lead sponsorTaipei Medical University Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposeother
Enrollment300
Start date20 December 2021
Primary completion31 December 2024
Estimated completion31 December 2024
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Taipei Medical University Hospital

Who can join

Adults 18 to 65, any sex, with Neuromuscular Blockade. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To shorten induction time, some anesthesiologist gives a priming dose of muscle relaxant before starting Neuromuscular Transmission monitor (NMT). To properly evaluate neuromuscular function during the surgury, baseline supramaximal stimulation of the monitored nerve is mandatory. Not knowing if the priming dose of muscle relaxant affects the supramaximal stimulation current setting, The investigators designed this study to find out.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Neuromuscular Blockade

Currently open trials in the same condition.

Other Taipei Medical University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05294523.

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