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Comparative Study of Baska & I-gel for Ventilation of Female Patients During Minor Procedures

NCT03140215 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2017-05-04

No results posted yet for this study

Summary

The study aimed to compare safety of the 3rd generation Supra-glottic airway device (SAD) "Baska" to the I-Gel , regarding seal pressure, fitting on the larynx (detected by Fiberoptic) \& complications. The study will be done for females undergoing minor gynecological procedures under general anesthesia with spontaneous ventilation.

Conditions

  • Medical Device Complication

Interventions

DEVICE

laryngeal mask insertion (Baska)

DEVICE

laryngeal mask insertion (I-gel )

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Nesrine A. El-Refai, M.D · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2016-12-31
Completion
2017-08-31

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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 NCT03140215 on ClinicalTrials.gov