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Evaluation of the Ambu® AuraGain in Ambulatory Surgery

NCT04501068 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2020-08-06

No results posted yet for this study

Summary

The study was designed to evaluate the success rate, time of insertion, sealing efficacy and security of the Ambu® AuraGain in patients undergoing ambulatory surgery by one anesthetist

Conditions

  • Airway

Interventions

DEVICE

Ambu® AuraGainTM

Evaluate the time of insertion, performance, security and insertion success rate of the Ambu® AuraGainTM in patients undergoing ambulatory surgery and general anaesthesia

Sponsors & Collaborators

  • Hospital General Universitario Gregorio Marañon

    lead OTHER

Principal Investigators

  • Javier Hortal, MD, PhD · Servicio de Anestesiología, Hospital General Universitario Gregorio Marañón

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2020-06-01
Completion
2020-06-01

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04501068 on ClinicalTrials.gov