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Neuromuscular Blockade clinical trials

View clinical trials related to Neuromuscular Blockade.

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NCT ID: NCT00660413 Completed - Clinical trials for Neuromuscular Blockade

Comparison of Acceleromyography (AMG) and Mechanomyography (MMG) for Establishing Potency of Neuromuscular Blocking Agents

Start date: December 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study was to compare two methods for neuromuscular monitoring, acceleromyography and mechanomyography for establishing the dose-response relationship and the potency of a neuromuscular blocking agent using rocuronium as an example. We hypothesized that there would be no significant difference between potencies estimated using acceleromyography and mechanomyography.

NCT ID: NCT00656799 Completed - Clinical trials for Neuromuscular Blockade

Dialysis of Sugammadex in Participants With Severe Renal Impairment (Study 19.4.333) (P05773)

Start date: April 2008
Phase: Phase 3
Study type: Interventional

The clinical trial objectives were to evaluate the dialysability of the sugammadex-rocuronium complex; it's safety and efficacy in participants with severe renal impairment.

NCT ID: NCT00620386 Completed - Clinical trials for Neuromuscular Blockade

Endotracheal Intubation Using Bonfils Fibrescope Without Neuromuscular Blockade

Start date: October 2006
Phase: Phase 2/Phase 3
Study type: Interventional

We studied intubating conditions and hemodynamic changes during endotracheal intubation employing either Bonfils intubating fiberscope or the conventional Macintosh laryngoscopy in 80 healthy patients candidates for elective surgery requiring endotracheal intubation. We omitted neuromuscular blocking drugs from the induction regimen.

NCT ID: NCT00535496 Completed - Clinical trials for Neuromuscular Blockade

Relation Between TOF-Watch® SX and a Peripheral Nerve Stimulator After 4.0 mg.Kg-1 Sugammadex (P05698)

Start date: September 2007
Phase: Phase 3
Study type: Interventional

The objective of the trial is to determine the relationship within a participant between the time to manual detection of the reappearance of the fourth twitch (T4) measured using a peripheral nerve stimulator (PNS) and the time to recovery of the fourth twitch/first twitch (T4/T1) ratio to 0.9 measured using a Train Of Four (TOF)-Watch® SX, of 4.0 mg/kg sugammadex administered at 15 minutes after either a bolus dose of 0.6 mg/kg rocuronium or the last maintenance dose of 0.15 mg/kg rocuronium.

NCT ID: NCT00472121 Completed - Clinical trials for Neuromuscular Blockade

The Precision and Arm-to-Arm Variation of Mechanomyography and Acceleromyography for Monitoring of Neuromuscular Block

Start date: May 2007
Phase: Phase 4
Study type: Observational

The purpose of the study is the examine the precision of acceleromyography and mechanomyography during recovery from a neuromuscular blocking agent and to examine whether there is any difference in monitoring block at the dominant or non-dominant arm. Our hypothesis is that there is no significant difference in neither the precision nor the level of block in the contralateral arms.

NCT ID: NCT00405977 Completed - Clinical trials for Neuromuscular Blockade

The Effect of Magnesium Sulphate on the Time Course of Rocuronium Induced Neuromuscular Block

MagRoc
Start date: May 2006
Phase: Phase 4
Study type: Interventional

The aim of this study is to investigate whether an optimized pre-treatment with intravenous magnesium enhances the speed of onset of a standard intubation dose of rocuronium.

NCT ID: NCT00390507 Completed - Clinical trials for Neuromuscular Blockade

Modification of Posttetanic Count (PTC) for Monitoring Deep Neuromuscular Block II

Start date: October 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the relationship between post-tetanic count (PTC) and time to first response to Train of four (TOF) stimulation during deep neuromuscular blockade induced by rocuronium.

NCT ID: NCT00226018 Completed - Clinical trials for Neuromuscular Blockade

Performance of Acceleromyography With and Without Preload

Start date: March 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the precision, bias and limits of agreement when monitoring the neuromuscular block with acceleromyography with and without preload and compare the method to the gold standard, mechanomyography.