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Clinical Trials/ACTRN12611000930987
ACTRN12611000930987
Completed
Phase 4

A single blinded, randomised controlled trial in women undergoing intermediate-duration gynaecological laparoscopy comparing the ProSeal (TM) laryngeal mask airway and the endotracheal tube.

Dr James Griffiths0 sites120 target enrollmentAugust 30, 2011

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr James Griffiths
Enrollment
120
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 30, 2011
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Dr James Griffiths

Eligibility Criteria

Inclusion Criteria

  • Adult female patients undergoing relaxant general anaesthesia for intermediate\-duration gynaecological laparoscopy

Exclusion Criteria

  • Anticipated surgical duration less than 30 minutes or greater than 120 minutes
  • Contraindications to the use of a LMA in laparoscopic surgery \- obesity, symptoms of gastroesophageal reflux, known or anticipated difficult airway
  • Contraindications to any study drug (including morphine and parecoxib)

Outcomes

Primary Outcomes

Not specified

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