ClinicalTrials.Veeva

Menu

Supreme LMA and Proseal LMA in Prone Anesthetized Patient (SPLMA)

P

Prince of Songkla University

Status

Unknown

Conditions

Inadequate or Impaired Breathing Pattern or Ventilation

Treatments

Device: Supreme LMA
Device: Proseal LMA

Study type

Interventional

Funder types

Other

Identifiers

NCT01814306
SPLMA-100
SPLMA-100-CPrechawai (Registry Identifier)

Details and patient eligibility

About

There is no significant difference about success rate of two devices.

Full description

There is no significant difference about success rate of two device: efficacy and safety

Enrollment

100 patients

Sex

All

Ages

Under 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • American Society Anesthesiologists physical status I-III
  • Patient undergo elective orthopedics surgery in prone position under general anaesthesia

Exclusion criteria

  • Age <15year
  • Non-fast
  • Morbid obesity (BMI > 35kg/m2)
  • Pregnancy
  • Known or predicted difficult airway
  • GERD
  • History of laryngeal problem (injury,subglottic stenosis)
  • Local pharyngeal problem (abscess,tumor)
  • Poor dentation
  • Pulmonary disease

Trial design

100 participants in 2 patient groups

Supreme
Active Comparator group
Description:
Supreme LMA
Treatment:
Device: Supreme LMA
Proseal
Active Comparator group
Description:
Proseal LMA
Treatment:
Device: Proseal LMA

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems