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NCT03219138

Algorithm of Muscle Function Tests to Detect Residual Neuromuscular Blockade.

Completed NA Last updated 17 July 2017
What this trial tests

NA trial testing Acceleromyography in Postoperative Residual Curarization in 265 participants. Completed in 25 July 2009.

Timeline
8 January 2008
Primary endpoint
25 July 2009
25 July 2009

Quick facts

Lead sponsorUniversity of Regensburg
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingsingle
Primary purposediagnostic
Enrollment265
Start date8 January 2008
Primary completion25 July 2009
Estimated completion25 July 2009
Sites5 locations across Germany

Drugs / interventions tested

Conditions studied

Sponsor

University of Regensburg

Who can join

Adults 18 to 65, any sex, with Postoperative Residual Curarization. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective neuromuscular monitoring is the gold standard to detect postoperative residual curarization (PORC). Many anesthesiologist just use qualitative neuromuscular monitoring or unreliable, clinical tests. Goal of this study is to develop an algorithm of muscle function tests to identify PORC

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Development of an algorithm using clinical tests to avoid post-operative residual neuromuscular block.
    Unterbuchner C, Blobner M, Pühringer F, Janda M, et al · · 2017 · cited 9× · PMID 28778151 · DOI 10.1186/s12871-017-0393-4

Verify or expand the search:

Other trials of Acceleromyography

Trials testing the same drug.

Other recruiting trials for Postoperative Residual Curarization

Currently open trials in the same condition.

Other University of Regensburg trials

Trials by the same sponsor.

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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/NCT03219138.

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