Clinical Trials Directory

Trials / Completed

CompletedNCT03568721

Postoperative Effects of Chewing Gum, Ibuprofen and Acetaminophen on Pain After Initial Archwire Placement

Postoperative Effects of Chewing Gum, Ibuprofen and Acetaminophen on Pain After Initial Archwire Placement: a Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
81 (actual)
Sponsor
Rio de Janeiro State University · Academic / Other
Sex
All
Age
12 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the efficacy of ibuprofen, acetaminophen, chewing gum in reducing orthodontic pain. This study include 81 patients to be classified into 4 groups of 19 each: ibuprofen (400 mg), acetaminophen (500 mg), chewing gum and control. The patients in each group will receive 1 method immediately after placement of the initial archwire and every 6 hours for a week if they experiences pain. Pain perception will be recorded by the patients while jaw rest position and fitting back teeth at 2 hours, 24 hours, 2 days, 3 days, 7 days and 21 days after archwire placement, using a visual analog scale.

Conditions

Interventions

TypeNameDescription
DRUGIbuprofenprescription of ibuprofen 400 mg
DRUGAcetaminophenprescription of acetaminophen 500 mg
OTHERChewing gumprescription of one tablet of chewing gum

Timeline

Start date
2015-01-25
Primary completion
2018-03-18
Completion
2018-05-20
First posted
2018-06-26
Last updated
2018-12-03

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT03568721. Inclusion in this directory is not an endorsement.