Clinical Trials

LMA Cuff Pressure and LMA-induced Complications

Location:

Trial status:

Open for Enrollment

Why is this study being done?

The purpose of this study is to determine if using 20 mL B.Braun syringes to inflate LMAs and allowing them to recoil will put the pressure of the LMA cuff within the safety range. It will also determine if remaining within this safety range has an effect on complications after surgery..

Who is eligible to participate?

Inclusion Criteria:

- Registered Mayo Clinic in Florida patients scheduled to undergo a surgery

- Planned use of LMA during surgery

- between the ages of 18-99

- short duration (<2 hours elective surgery)

Exclusion Criteria:

- recent history of upper respiratory tract infection

- intra-cavitary or laparoscopic procedure

- risk of pulmonary aspiration

- known difficult airway

- history of gastric reflux

- BMI > 40

- lateral or prone positions

- oral or nasal surgery

Last updated: 01/08/2013

NCT ID: NCT01385969

IRB Number:11-001506