Clinical Trials Directory

Trials / Completed

CompletedNCT01651572

Comparison Between Cisatracurium and Rocuronium in Terms of Recovery of the Muscular Strength in the Postoperative Phase After Surgery and General Anaesthesia

Assessment of Post-operative Residual Curarization (PORC) Incidence in Patients Undergoing Surgery With General Anaesthesia; Comparison Between Cisatracurium and Rocuronium. A Randomised, Single-blind Phase 4 Study.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Azienda Ospedaliera di Padova · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the incidence of post-operative residual curarization in our patients and to determine if Cisatracurium and Rocuronium behave differently from each other in terms of residual curarization.

Conditions

Interventions

TypeNameDescription
DRUGCisatracuriumCisatracurium (Nimbex): * initial dose: 0.2 mg/kg * maintaining dose: 0.1 mg/kg (repeated anytime TOF-count reaches 2 twitches)
DRUGRocuroniumRocuronium (Esmeron): * initial dose: 0.6 mg/kg * maintaining dose: 0.15 mg/kg (repeated anytime TOF-count reaches 2 twitches)

Timeline

Start date
2012-07-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2012-07-27
Last updated
2014-03-11

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01651572. Inclusion in this directory is not an endorsement.