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DPBRN Peri-operative Pain and Root Canal Therapy

NCT01201681 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2011-09-20

No results posted yet for this study

Summary

The purpose of this study is to identify pre-operative factors that put patients at greater risk of developing severe tooth pain following root canal therapy, thereby providing evidence that will allow dentists to act preventively to lessen this risk, improve pain control, increase their patients' quality of life, and decrease the number of dental emergency interactions.

A parallel goal of this study is to assess the feasibility of recruiting dentists that provide root canal therapy and patients using the DPBRN.

Conditions

  • Post-operative Tooth Pain
  • Root Canal Therapy

Sponsors & Collaborators

  • National Institute of Dental and Craniofacial Research (NIDCR)

    collaborator NIH

  • HealthPartners Institute

    collaborator OTHER

  • Kaiser Permanente

    collaborator OTHER

  • Permanente Dental Associates Group, Oregon

    collaborator OTHER

  • University of Florida

    collaborator OTHER

  • University of Copenhagen

    collaborator OTHER

  • University of Alabama at Birmingham

    collaborator OTHER

  • University of Minnesota

    collaborator OTHER

  • Dental Practice-Based Research Network

    lead NETWORK

Principal Investigators

  • Donald R Nixdorf, DDS, MS · University of Minnesota

Eligibility

Min Age
19 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2011-09-30
Completion
2011-09-30

Countries

  • United States
  • Denmark

Study Locations

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Entities

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01201681 on ClinicalTrials.gov