Trials / Completed
CompletedNCT02820792
Non-Crossover Study of the LMA Protector Versus Ambu AuraGain
A Randomized Non-Crossover Study of the LMA ProtectorTM Versus Ambu Aura GainTM in Adult Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 96 (actual)
- Sponsor
- Schulthess Klinik · Academic / Other
- Sex
- All
- Age
- 19 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The LMA ProtectorTM is a new extraglottic airway device which brings together features of both the LMA ProSealTM (high seal cuff, gastric access and bite block - to facilitate ventilation, airway protection and airway obstruction, respectively) and the LMA UniqueTM (single use - prevention of disease transmission). In the following randomized study the investigators test the hypothesis that ease of insertion, oropharyngeal leak pressure, fiberoptic position and ease of gastric tube placement differ between the LMA ProtectorTM and the Ambu AuraGainTM in paralyzed, anesthetized patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | function tests | function tests: ease of insertion, oropharyngeal seal pressure, fiberoptic position, ease of ventilation, occult blood, gastric tube insertion |
| DEVICE | LMA ProtectorTM | |
| DEVICE | Ambu AuraGainTM |
Timeline
- Start date
- 2016-09-01
- Primary completion
- 2016-12-01
- Completion
- 2016-12-20
- First posted
- 2016-07-01
- Last updated
- 2017-01-26
Locations
2 sites across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT02820792. Inclusion in this directory is not an endorsement.