CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 80 enrolled
Drug / intervention
Neostigmine (40 mcg / kg) at different time of neuromuscular block's recovery +1 moredrug
Likely dose
Neostigmine (40 mcg / kg) at different time of neuromuscular block's recoveryfrom record
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Search/NCT03019835
NCT03019835N/ACompleted

Can we Antagonize Mivacurium With Neostigmine

Université Libre de Bruxelles·interventional·Posted Jan 13, 2017·Updated May 19, 2017

In Brief

A clinical study evaluating Neostigmine (40 mcg / kg) at different time of neuromuscular block's recovery and Spontaneous recovery for Mivacurium and 2 related conditions. Completed, enrolled 80 participants across 1 site.

Detailed Summary

The antagonism of neuromuscular blocking agents (NMBA) (or curares), as well as the antagonism of other drugs used in anesthesia, is a major challenge for the speciality. Residual paralysis is indeed a risk factor for post-operative morbidity and mortality and antagonization of curares at the end of the procedure is associated with a reduction in mortality . Its use should be as large as possible and its contraindications are extremely rare. The antagonism of the NMBA reduces the duration of the neuromuscular block and the complications that are associated . In this study, the investigators use mivacurium (or Mivacron) as non-depolarizing curare and neostigmine as an antagonist. Neostigmine reduces the duration of the neuromuscular block induced by mivacurium, By reducing the breakdown of acetylcholine, neostigmine induces an increase in acetylcholine in the synaptic cleft which competes for the same binding site as nondepolarizing neuromuscular blocking agents, and reverses the neuromuscular blockade. But the use of neostigmine in current practice is not very widespread in this clinical situation. The reduction in the duration of the block is significant in comparison with a spontaneous recovery . Moreover, spontaneous recovery is not always complete and sometimes very long. Nevertheless, its action is effective and this study could support this use but also specify the duration and the quality of the return to normal of the neuromuscular transmission.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJan 13, 2017
Enrollment StartDec 1, 2016
Primary CompletionApr 22, 2017
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 9.5 years ago

Interventions

Neostigmine (40 mcg / kg) at different time of neuromuscular block's recoverydrug

Spontaneous recoveryother

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