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Clinical Trials/CTRI/2016/04/006833
CTRI/2016/04/006833Not yet recruitingPhase 4

Comparative evaluation of Air-Q Blocker and ProSeal Laryngeal Mask Airway in patients undergoing elective surgery under general anaesthesia.

Government Medical College0 sites90 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Enrollment
90
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •The following patients will be included in the study
  • •1.Age group between 18 to 60 years
  • •2.American Society of Anaesthesiologist (ASA) physical status I and II
  • •3.Patients scheduled for elective surgery under general anaesthesia (Duration of surgery 2 ± 0.5 hrs)

Exclusion Criteria

  • •The following patients will be excluded from the study
  • •1.Patients with anticipated difficult airway (Airway Difficulty Score >8) 25
  • •2.Patients with upper respiratory tract infection
  • •3.Patients with increased risk of regurgitation and aspiration of gastric content
  • •4.Patients with a body mass index (BMI) > 35 kg.m.-2
  • •5.Patients with past history of radiotherapy to the neck involving the hypopharynx
  • •6.Patients undergoing surgeries involving neck and oral cavity
  • •7.Pregnant patients

Investigators

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