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DPBRN Peri-operative Pain and Root Canal Therapy

Peri-operative Pain and Root Canal Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01201681
Enrollment
500
Registered
2010-09-14
Start date
2010-07-31
Completion date
2011-09-30
Last updated
2011-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-operative Tooth Pain, Root Canal Therapy

Keywords

Post-operative pain, intra-operative pain, root canal therapy, feasibility, post-surgical persistent pain

Brief 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.

Detailed description

Goals for this study is to: * Assess the frequency and intensity of pre-operative pain * Evaluate the occurence and intensity of intra-operative pain * Evaluate the occurence and intensity of post-operative pain * Assess the interference of persistent tooth pain with daily life * Identify a limited set of risk factors related to the development of post-operative pain.

Interventions

None listed

Sponsors

National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
HealthPartners Institute
CollaboratorOTHER
Kaiser Permanente
CollaboratorOTHER
Permanente Dental Associates Group, Oregon
CollaboratorOTHER
University of Florida
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
University of Alabama at Birmingham
CollaboratorOTHER
University of Minnesota
CollaboratorOTHER
Dental Practice-Based Research Network
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* 19-70 years old * permanent adult tooth requiring it first non-surgical root canal therapy * patients with more than 1 tooth requiring root canal therapy are eligible, but only the first root canal procedure performed will be included to avoid problems of correlation within patients

Exclusion criteria

* Evidence of prior root canal therapy, including iatrogenic, but not disease-induced, pulp access of the tooth being considered * patients with obvious cognitive impairments (e.g., past stroke with communication deficits, dementia, mental disability) * patients unable to return for 6 month follow-up, since another study plans to obtain data of these patients at that time (DPBRN Persistent Tooth Pain)

Countries

Denmark, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026