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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00223470
Other study ID # 012-1904-455
Secondary ID K23DE014864-01A1
Status Completed
Phase N/A
First received September 13, 2005
Last updated March 7, 2012
Start date October 2002
Est. completion date June 2008

Study information

Verified date March 2012
Source The University of Texas Health Science Center at San Antonio
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

This clinical trial evaluates the role of cytokines in patients needing root canal treatment with diagnosis of necrotic pulp and chronic apical periodontitis


Description:

This study evaluates whether periradicular exudate concentrations of cytokines differ in patients experiencing pain and mechanical allodynia due to pulpal necrosis with an acute exacerbation of a chronic apical periodontitis, as compared to patients with pulpal necrosis with chronic apical periodontitis, but no pain or mechanical allodynia


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender Both
Age group 16 Years to 60 Years
Eligibility Inclusion Criteria:

1. Patient must be at least 16 years of age.

2. Clinical indication for Non-Surgical Root Canal Therapy (NSRCT).

3. 1st or 2nd maxillary or mandibular molar

4. Diagnosis must be Chronic Apical Periodontitis (CAP) with or without symptoms.

5. Intact, mature apices.

6. ASA I or II

Exclusion Criteria:

1. Failure to meet any of the above

2. Previous NSRCT

3. Previous pulpotomy or pulpectomy

4. Suppurative apical periodontitis

5. Patients taking medications which can affect their pain rating or medications which effect their immune system ( such as glucocorticoids)

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Univerity of Texas Health Science Center at San Antonio San Antonio Texas

Sponsors (3)

Lead Sponsor Collaborator
The University of Texas Health Science Center at San Antonio National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

See also
  Status Clinical Trial Phase
Completed NCT00223379 - Longitudinal Endodontic Study of Apical Preparation Size N/A