NCT03809507

Brief Summary

Under the auspices of the Oral Health Section of the NC Department of Health and Human Services clinician-investigators from the UNC Oral and Maxillofacial Surgery Department are conducting a survey to assess current analgesic prescribing practices in NC with a goal of eventually reaching consensus among clinicians for a wide range of procedures and conditions where pain control is important for successful patient outcomes. We hope that about 850 dentists and 600 physicians will agree to take part in this research study. Participation in this Qualtrics survey e-mailed in mid-February 2019 will take about 15 minutes or less.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
895

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2019

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 15, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 18, 2019

Completed
3 months until next milestone

Study Start

First participant enrolled

April 5, 2019

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2021

Completed
Last Updated

September 30, 2021

Status Verified

September 1, 2020

Enrollment Period

2.3 years

First QC Date

January 15, 2019

Last Update Submit

September 29, 2021

Conditions

Keywords

opioids

Outcome Measures

Primary Outcomes (1)

  • Number of Clinicians Prescribing Opioid Drugs for each Survey Scenario

    Qualtrics Survey of NC Clinicians with DEA registration. Yes/No responses for opioid drug prescribing for 2 to 3 scenarios differing by target group of clinicians will be asked of 6 different clinician types, emergency room physicians, general dentists and dental specialists..

    one year

Study Arms (1)

NC Clinicians

Qualtrics Survey of NC Clinicians with DEA registration

Other: Qualtrics survey questions

Interventions

Qualtrics Survey: For each of the scenarios, practitioners will be asked whether opioids are prescribed or not, and the type(s) of other analgesic medications that would be prescribed, the strength in mg, and the number of doses for each medication

NC Clinicians

Eligibility Criteria

Age25 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

General dentists, Endodontists, Periodontists, Oral and Maxillofacial Surgeons. Emergency Room Physicians

You may qualify if:

  • NC licensed dentists or physicians with active DEA registration.

You may not qualify if:

  • NC licensed dentists or physicians with no active DEA registration.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of North Carolina School of Dentistry

Chapel Hill, North Carolina, 27599-7450, United States

Location

Study Officials

  • Raymond P White, Jr, DDS. PhD

    Oral and Maxillofacial Surgery, UNC School of Dentistry

    STUDY DIRECTOR
  • Glenn Reside, DMD

    Oral and Maxillofacial Surgery, UNC School of Dentistry

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 15, 2019

First Posted

January 18, 2019

Study Start

April 5, 2019

Primary Completion

July 31, 2021

Study Completion

August 31, 2021

Last Updated

September 30, 2021

Record last verified: 2020-09

Data Sharing

IPD Sharing
Will share

Deidentified data that supports results will be shared provided the investigator who proposes use of the data has Institutional Review Board(IRB), Independent Ethics Committee, or Research Ethics Board, as applicable, and executes a data use/sharing agreement with UNC

Shared Documents
STUDY PROTOCOL, CSR
Time Frame
beginning 9 to 36 months following publication
Access Criteria
Institutional Review Board(IRB), Independent Ethics Committee, or Research Ethics Board, as applicable, and executes a data use/sharing agreement with UNC
More information

Locations