# The i-GelTM. A Randomized, Crossover Study With the Laryngeal Mask Airway ProSealTM in Anesthetized Pediatric Patients

> **NCT01425151** · NA · COMPLETED · sponsor: **Schulthess Klinik** · enrollment: 60 (estimated)

## Conditions studied

- Device Success Rate
- Device Performance

## Interventions

- **DEVICE:** i-Gel
- **DEVICE:** ProSeal

## Key facts

- **NCT ID:** NCT01425151
- **Lead sponsor:** Schulthess Klinik
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2010-01
- **Primary completion:** 2011-09
- **Final completion:** 2011-09
- **Target enrollment:** 60 (ESTIMATED)
- **Last updated:** 2011-09-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01425151

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01425151, "The i-GelTM. A Randomized, Crossover Study With the Laryngeal Mask Airway ProSealTM in Anesthetized Pediatric Patients". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT01425151. Licensed CC0.

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