Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00528502

Lidocaine Supplement for Minimal Invasive Parathyroid Surgery

Prevention of Laryngeal Reflexes in Minimal Invasive Parathyroid Surgery by the Use of Topical Lidocaine

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
M.D. Anderson Cancer Center · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Primary Objective: 1\. To determine if the application of lidocaine to the airway will obtund or abolish the laryngeal reflexes. This in turn will lead to a quiescent controlled surgical field.

Detailed description

Lidocaine is a local anesthetic that causes numbness to the throat when misted into the air. This numbness in the throat should stop the urge to clear the throat in the middle of the operation. Therefore, this should stop the interruptions during the surgery. If you agree to take part in this study, you will be randomly assigned (as in the toss of a coin) to one of 2 groups. Participants in Group 1 will receive the saline mist. This will moisturize and soothe the throat. Participants in Group 2 will receive the lidocaine mist. Lidocaine or saline is misted into the air that you breathe during the surgery. You and your surgeon will not be told which group you were assigned to. At the end of the surgery, your surgeon will answer some questions to help determine if the use of lidocaine or saline is beneficial. You will be considered off-study once you are sent to the recovery room after surgery. This is an investigational study. Lidocaine is FDA-approved and commercially available for local anesthesia. If you are in the lidocaine or the saline group. Up to 105 patients will take part in this study. All will be enrolled at M. D. Anderson.

Conditions

Interventions

TypeNameDescription
DRUGLidocaineLidocaine is misted into the air that you breathe during the surgery.
DRUGSalineSaline is misted into the air that you breathe during the surgery.

Timeline

Start date
2006-06-01
Primary completion
2008-01-01
Completion
2008-01-01
First posted
2007-09-12
Last updated
2012-12-07

Source: ClinicalTrials.gov record NCT00528502. Inclusion in this directory is not an endorsement.