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Clinical Trials/NCT03456141
NCT03456141
Completed
N/A

Prospective, Observational Study With a Multimodal Analgesic Protocol to Moderate Acute Pain After Third Molar Surgery

University of North Carolina, Chapel Hill1 site in 1 country100 target enrollmentMarch 1, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Pain, Post-operative
Sponsor
University of North Carolina, Chapel Hill
Enrollment
100
Locations
1
Primary Endpoint
The impact of the surgery on the patient's post-surgery pain.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

With a prospective, observational study assess post-surgery pain levels and patient's use of opioids and other analgesic drugs to moderate pain following third molar surgery.

Detailed Description

SPECIFIC AIMS Using the UNC surgery clinic multi-modal protocol of drugs/dosages to control acute pain after third molar surgery assess each post-surgery day(PSD) the patient reported 1. pain levels post-surgery as recorded by Likert-type and Gracely scales 2. quality of life(QOL) outcomes for lifestyle and oral function 3. number of opioid doses taken by subject-patients 4. number of NSAID and acetaminophen doses taken by subject-patients.

Registry
clinicaltrials.gov
Start Date
March 1, 2018
End Date
December 31, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ASA I,II At least two lower 3rd molars scheduled for removal

Exclusion Criteria

  • Patient being treated for opioid addiction/abuse including having Rx for suboxone, methadone

Outcomes

Primary Outcomes

The impact of the surgery on the patient's post-surgery pain.

Time Frame: 14 days

Likert scales for average pain and worst pain are assessed with 7-point scales with verbal anchors of "no pain" and "worst pain imagined". Recovery for pain on the Likert scales is defined as the number of PSD until the patient reports a score of 1 or 2 on the 7-point scale.

Study Sites (1)

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