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Clinical Trials/EUCTR2013-001965-17-HU
EUCTR2013-001965-17-HU
Active, not recruiting
Not Applicable

Incidence of postoperative residual neuromuscular blockade following the administration of rocuronium: A randomized placebo controlled study.

Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék0 sitesAugust 6, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
The effect of sugammadex and neostigmin on postoperative residual neuromuscular blockade will be investigated, therefore the patients suffering from various conditions undergoing surgery in general anaesthesia with muscle relaxation will be included int he study.sthesia with muscle relaxation will be included in the study.
Sponsor
Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék
Status
Active, not recruiting
Last Updated
12 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 6, 2013
End Date
TBD
Last Updated
12 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék

Eligibility Criteria

Inclusion Criteria

  • signed written informed consent sheet
  • \- age 18\-65 years
  • \- ASA I\-III (American Society of Anesthesiologists physical score)
  • \- BMI 18,5\-25 (normal body weight)
  • \- expected opration time at least 50 minutes
  • \- operation requiring intratracheal intubation
  • \- patient in supine position and one arm is accessible
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes

Exclusion Criteria

  • \- diseases affecting neuromuscular transmission (myasthenia, myopathy, stroke, severe hepatic or renal insufficiency)
  • \- medications affecting neuromuscular transmission (aminoglycoside antibiotics, magnesium)
  • \- difficult airway, difficult intubation expected
  • \- gravidity
  • \- lactation\- acute surgery
  • \- glaucoma
  • \- patient participated in an other trial within one month

Outcomes

Primary Outcomes

Not specified

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