Skip to main content
MedPath Trial logoMedPath TrialMedPath Trial Home
Clinical Trials/NCT03456141
NCT03456141CompletedNot Applicable

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 enrollmentStarted: March 1, 2018Last updated:
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
The impact of the surgery on the patient's post-surgery pain.
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Not yet recruiting
Not Applicable
Study on the Effects of Multimodal Analgesia Regimens on Postoperative Analgesia and Gastrointestinal Function Recovery After Laparoscopic Abdominal SurgeryLaparoscopic Abdominal Surgery
NCT06772545Xiaguang Duan120
Completed
Not Applicable
Pain and Narcotic Usage After Orthopaedic SurgeryFractures, ClosedPain, PostoperativePain CatastrophizingPain, AcuteAnalgesiaOpioid UseAcceptance and Commitment TherapyOrthopedicsAnalgesics, OpioidText Messaging
NCT03991546Christopher Anthony82
Withdrawn
Phase 1
A Study of Postsurgical Pain Control for Lower Extremity FracturesLower Extremity Fractures.
NCT02214810Broward Health
Terminated
Phase 4
Postoperative Opioid Use and Pain Scores in Patients Undergoing Transforaminal Lumbar Interbody FusionLow Back Pain
NCT02061774Texas Tech University Health Sciences Center21
Terminated
Phase 4
Phase 4 Study in Adult Subjects Undergoing Posterior Lumbar Spine SurgeriesPostoperative Pain Management
NCT03927911Pacira Pharmaceuticals, Inc65