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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03939936
Other study ID # 17-KAEK-44
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2017
Est. completion date February 15, 2018

Study information

Verified date May 2019
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is a relationship between psoriasis and periodontal disease. This relationship may be double-sided.


Description:

The aim of this randomized controlled clinical study was to determine the effect of non-surgical mechanical periodontal treatment on psoriasis. The study population consisted of 92 periodontitis patients with psoriasis who had untreated periodontal disease. Two randomized groups were formed from these patients. Immediate periodontal treatment (test group, n = 46) and delayed periodontal treatment (control group, n = 46). Clinical periodontal measures, saliva interleukin 2, interleukin 6 and secretory immunoglobulin A levels and PASI scores were performed at baseline and 8th week in control and test group.


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date February 15, 2018
Est. primary completion date January 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- the presence at least 20 remaining teeth,

- the presence of Stage I or Stage II Periodontitis,

- the presence of diagnosed psoriasis.

Exclusion Criteria:

- patients who had the immune-inflammatory disease and require antibiotic prophylaxis,

- patients who received periodontal treatment prior to 6 months,

- women who were breastfeeding or pregnant,

- patients using medicines such as antibiotics, anti-inflammatory drugs, immune-suppressants.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Psoriatic measurements
Psoriasis Area and Severity Index (PASI) was performed baseline and after 8 weeks. Saliva samples were taken from patients for the evaluation of proinflammatory cytokine baseline and after 8 weeks.
Non-surgical periodontal treatment
Non-surgical periodontal treatment was performed baseline and after 8 weeks. Saliva samples were taken from patients for the evaluation of proinflammatory cytokine baseline and after 8 weeks.
saliva samples
Saliva samples were taken from patients for the evaluation of proinflammatory cytokine baseline and after 8 weeks.

Locations

Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)

Lead Sponsor Collaborator
Ozge Gokturk

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proinflammatory cytokines The changes in proinflammatory cytokines levels within 8 weeks. Higher values represent a worse outcome. The decrease in proinflammatory cytokines levels is expected after periodontal treatment. Baseline and after 8 weeks
Secondary Gingival index The changes in gingival index level after periodontal treatment. Gingival index was measured for determining the severity of disease and clinical outcome. Higher values represent a worse outcome. After periodontal treatment, a reduction in gingival index value is expected. Baseline and after 8 weeks
Secondary PASI index The changes in PASI index level after periodontal treatment. PASI index was measured for determining the severity of psoriasis disease. Higher values represent a worse outcome. After periodontal treatment, a reduction in PASI index value is expected. Baseline and after 8 weeks
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