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NCT01035021 Clinical Trial

Neuromuscular Block in Laryngeal Mask Airway(LMA) Insertion

General Anesthesia Clinical Trial

Official title:
Effect of Neuromuscular Blockade on the Insertion of ProSeal™ Laryngeal Mask Airway and Postoperative Pharyngolaryngeal Discomfort

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01035021
Other study ID # LMA_M_relax
Secondary ID
Status Completed
Phase N/A
First received December 17, 2009
Last updated November 14, 2013
Start date June 2009
Est. completion date April 2010

Study information
Verified date November 2013
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the success rate, insertion time and complication depending on the use of neuromuscular blocking agent when inserting the laryngeal mask airway (LMA).

Recruitment information / eligibility
Status Completed
Enrollment 160
Est. completion date April 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 18-70 year

- american society of anesthesiologist status 1-2

- elective general anesthesia

Exclusion Criteria:

- known or predicted difficult airway

- recent sore throat

- mouth opening less than 2.5 cm

- at risk of aspiration

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• use of rocuronium when the LMA is inserted
Anesthesia is induced with a propofol and remifentanil in both groups, however rocuronium 0.06 mg/kg is injected only in group R. Insertion of LMA is performed by the standard technique according to the manufacturer's instruction. In group N, rocuronium is administered for the operation.

Locations
Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary success rate and insertion time when laryngeal mask airway is inserted
Secondary complication after the remove of LMA - bleeding, sore throat 1 hour after the LMA is removed
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