Trials / Completed
CompletedNCT01425151
The i-GelTM. A Randomized, Crossover Study With the Laryngeal Mask Airway ProSealTM in Anesthetized Pediatric Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Schulthess Klinik · Academic / Other
- Sex
- All
- Age
- 18 Months – 6 Years
- Healthy volunteers
- Not accepted
Summary
In the following randomized, crossover study, the investigators test the hypothesis that ease of insertion and oropharyngeal leak pressure differ between the LMA ProSealTM and the i-GelTM in anesthetized pediatric patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | i-Gel | Oropharyngeal leak pressure Insertion success |
| DEVICE | ProSeal | Oropharyngeal leak pressure Insertion success |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2011-09-01
- Completion
- 2011-09-01
- First posted
- 2011-08-29
- Last updated
- 2011-09-22
Locations
2 sites across 2 countries: Austria, Switzerland
Source: ClinicalTrials.gov record NCT01425151. Inclusion in this directory is not an endorsement.