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Comparison of ProSeal Laryngeal Mask Airway, LTS-D and I-gel in Mechanically Ventilated Patients

NCT02877940 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2016-08-24

No results posted yet for this study

Summary

The Aim of the study is to compare the clinical performance of p-LMA, i-gel and LTS-D in terms of the efficacy and safety in anaesthetized patient on Mechanical ventilation undergoing elective surgical procedure.

Conditions

  • Airway Morbidity

Interventions

DEVICE

ProSeal Laryngeal mask airway

ProSeal was inserted in mechanically ventilated patients undergoing elective surgeries.

DEVICE

Laryngeal Tube Suction- Disposable

LTS-D was inserted in mechanically ventilated patients undergoing elective surgeries.

DEVICE

i-gel

i-gel was inserted in mechanically ventilated patients undergoing elective surgeries.

Sponsors & Collaborators

  • Government Medical College, Haldwani

    lead OTHER

Principal Investigators

  • Geeta Bhandari, MD · Professor

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2016-06-30
Completion
2016-08-31

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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 NCT02877940 on ClinicalTrials.gov