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Using Dexamethasone After Uvulopalatopharyngoplasty

University of Oklahoma (OU) logo

University of Oklahoma (OU)

Status and phase

Completed
Phase 1

Conditions

Pain

Treatments

Drug: Placebo
Drug: Dexamethasone

Study type

Interventional

Funder types

Other

Identifiers

NCT00584168
UPPP Study, IRB # 12098 (Other Identifier)
Dexamethasone, UPPP - Houck

Details and patient eligibility

About

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

Full 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.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Candidates scheduled for UPPP surgery.
  • Able to take steroids

Exclusion criteria

  • Those patients who unable to take steroids

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

15 participants in 2 patient groups, including a placebo group

2
Placebo Comparator group
Description:
Patient will receive a placebo.
Treatment:
Drug: Placebo
1
Experimental group
Description:
Patient will receive dexamethasone.
Treatment:
Drug: Dexamethasone

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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