Clinical Trials Logo

Clinical Trial Summary

Rocuronium is a aminosteroid structured, non-depolarizing neuromuscular blocking agents (NMB). Epidemiological data presents that the frequency of hypersensitivity reactions caused by rocuronium have been increased. Determinations of serum tryptase concentrations are interdisciplinary recommended in diagnosis of its adverse reactions. No studies have been performed to explain specific role of rocuronium doses on serum tryptase values. The aim of this study was to investigate the potential effect of rocuronium on serum tryptase concentrations.


Clinical Trial Description

The greatest risk of hypersensitivity occurs during anesthesia for female patients and it is connected with the induction phase using skeletal muscle relaxants . Epidemiological data presents that the frequency of hypersensitivity reactions caused by rocuronium have been increased. Due to the multiple advantages reports of triggering allergic or hypersensitivity reactions caused by rocuronium create doubts about the safety of application . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04035707
Study type Interventional
Source Medical University of Bialystok
Contact
Status Completed
Phase N/A
Start date June 25, 2009
Completion date May 15, 2014

See also
  Status Clinical Trial Phase
Terminated NCT02185651 - A Pilot Study of Zavesca® in Patients With Pompe Disease and Infusion Associated Reaction Phase 1
Completed NCT02349763 - Dexamethasone Regimens for Prophylaxis of Paclitaxel-associated Hypersensitivity Reaction Phase 3