Skip to content

DPBRN Persistent Pain and Root Canal Therapy

Persistent Pain and Root Canal Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01201668
Enrollment
500
Registered
2010-09-14
Start date
2010-08-31
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

Persistent Tooth Pain, Root Canal Therapy

Keywords

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

Brief summary

The purpose of this study is to document by survey the occurence of tooth pain present 3 months and 6 months after root canal therapy in the patients recruited for the DPBRN Peri-operative tooth pain study. This study will access the feasibility of obtaining 3 month and 6 month follow-up data on the patient enrolled in the DPBRN Peri-operative tooth pain study.

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 Copenhagen
CollaboratorOTHER
University of Florida
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
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* 19-70 years old * Permanent adult tooth requiring its 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 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

Countries

Denmark, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026