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NCT01153152 Clinical Trial

Study of Pain Following Removal of Wisdom Teeth With Acute Pulpitis

Pain Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01153152
Other study ID # NO.2009128
Secondary ID
Status Completed
Phase N/A
First received June 28, 2010
Last updated June 28, 2010
Est. completion date September 2009

Study information
Verified date February 2009
Source Wuhan University
Contact n/a
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether pulp chamber opening and drainage on wisdom teeth with acute pulpitis before the extraction could reduce postoperative pain so beneficial to patient.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date September 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 29 Years
Eligibility Inclusion Criteria:

- inclusion criteria of upper wisdom teeth for the two groups were: vertical eruption; being worthless to be restored; deep caries in the occlusion surface with acute pain; without caries or acute pulpitis in the adjacent second molar

Exclusion Criteria:

- systemic diseases, smokers, inflammation in oral cavity,with history of psychiatric illness,pregnant or lactating females

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
China School and Hospital of Stomatology, Wuhan University Wuhan Hubei

Sponsors (1)
Lead Sponsor Collaborator
Wuhan University

Country where clinical trial is conducted

China, 

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