Clinical Trials Directory

Trials / Completed

CompletedNCT00584168

Using Dexamethasone After Uvulopalatopharyngoplasty

Decreasing Morbidity After Uvulopalatopharyngoplasty With the Use of Dexamethasone - A Randomized Double Blinded Placebo Controlled Trial

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
University of Oklahoma · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study looks at lessening the pain after a Uvulopalatopharyngoplasty (UPPP) surgery by using Dexamethasone (a corticosteroid).

Detailed description

The study was designed because patients have a lot of pain after they have a UPPP. Certain drugs called steroids may lessen the pain associated from this surgery. This study uses Dexamethasone (a corticosteroid), to see if it will help reduce pain, decrease the amount of time until the patient can begin to eat or return to normal activity, or increase their satisfaction with pain management. In this study the patients will be randomized (computer chosen) to receive either the study drug (dexamethasone), or a placebo. The patient will start the day before surgery with a single pill. They will then receive the dexamethasone or a placebo twice daily for the next four days and then once daily for the next two days for a total of seven days. Afterward, they will be asked to complete a questionnaire. The five questions ask patients to access the amount of pain they have, how much of their normal diet or activity they have returned to, and how much pain medication they have taken. At the next follow-up visit they will be asked to complete another questionaire (9 questions) about the patient's satisfaction with pain management.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneThey will take a pill the day before surgery, twice daily for the next four days and then once daily for the next two days for a total of seven days.
DRUGPlaceboThey will take a pill the day before surgery, twice daily for the next four days and then once daily for the next two days for a total of seven days.

Timeline

Start date
2005-03-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2008-01-02
Last updated
2012-02-02

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00584168. Inclusion in this directory is not an endorsement.