Trials / Completed
CompletedNCT02318810
Influence of the Neuromuscular Blockade on Mask Ventilation
The Influence of the Neuromuscular Blockade on Mask Ventilation; a Placebo Controlled, Randomized Trial With Three Different Dosages of Rocuronium (0.3 mg/kg, 0.6 mg/kg and 0.9 mg/kg)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (actual)
- Sponsor
- University of Rostock · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Mask ventilation during induction of anesthesia can be improved by administration of neuromuscular blocking agents (NMBAs). NMBAs are usually administered after testing mask ventilation; however, muscle relaxants may improve mask ventilation and they do not alter mask ventilation. Thus, growing evidence suggests to administer muscle relaxants before testing mask ventilation. We will study different dosages of rocuronium; we assume that higher dosages of rocuronium will improve mask ventilation compared with lower dosages.
Detailed description
Mask ventilation during induction of anesthesia can be improved by administration of neuromuscular blocking agents (NMBAs). NMBAs are usually administered after testing mask ventilation; however, muscle relaxants may improve mask ventilation and they do not alter mask ventilation. Thus, growing evidence suggests to administer muscle relaxants before testing mask ventilation.We will administer rocuronium 0.3 mg/kg, 0.6 mg/kg, 0.9 mg/kg and saline (placebo group) before starting with mask ventilation. We will grade mask ventilation based on various scores before and after rocuronium application. Afterwards patient's tracheas will be intubated. We assess risk factors for difficult mask ventilation. We hypothesize that rocuronium 0.9 mg/kg will be superior to rocuronium 0.3 mg/kg and saline.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rocuronium 0.3 mg/kg | Patients receive rocuronium 0.3 mg/kg |
| DRUG | Rocuronium 0.6 mg/kg | Patients receive rocuronium 0.6 mg/kg |
| DRUG | Rocuronium 0.9 mg/kg | Patients receive rocuronium 0.9 mg/kg |
| DRUG | Placebo | Patients receive saline |
Timeline
- Start date
- 2015-03-01
- Primary completion
- 2016-05-01
- Completion
- 2016-05-01
- First posted
- 2014-12-17
- Last updated
- 2016-05-03
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT02318810. Inclusion in this directory is not an endorsement.