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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06140394
Other study ID # P-ME-23-04
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 29, 2023
Est. completion date June 29, 2024

Study information

Verified date November 2023
Source Faculty of Dental Medicine for Girls
Contact Alaa HM Naguib, bachelor's
Phone 01004962573
Email dr.alaaelbarahmtouchy@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the summary is to evaluate The Effect of Low-Level Laser Therapy as an Adjunct to Non-surgical Therapy on Inducible Nitrous Oxide Synthase Salivary Levels in Different Age Groups of Chronic Periodontitis Patients


Description:

2 ml of unstimulated saliva will be collected using spitting method, the collected samples will then be analyzed using Elisa technique for salivary Inducible nitrous oxide synthase levels.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date June 29, 2024
Est. primary completion date April 29, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria: - males and females - aged below 40 or above 60 - periodontitis stage 2 - no tooth loss due to periodontitis Exclusion Criteria: - smoking habits - history of antibiotics - history of systemic diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
diode laser
low level diode therapy
non surgical scaling
non surgical scaling using ultrasonic

Locations

Country Name City State
Egypt Al-Azhar University Cairo Nasrcity Nasr Street
Egypt Hamdy Nassar Cairo

Sponsors (1)

Lead Sponsor Collaborator
Faculty of Dental Medicine for Girls

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical parameters (gingival index) measurement if the gingival index using scoring system. A score from 0.1-1.0 = mild inflammation; 1.1-2.0 = moderate inflammation from, and 2.1-3.0 signifies severe inflammation. 6 months
Primary clinical parameters (clinical attachment loss) measurement of clinical parameters clinical attachment loss in millimeters 6 months
Secondary assessment of inducible nitrous oxide synthase levels measurement of inducible nitrous oxide synthase levels in different age groups before the procedure and after using Elisa kit. 3 months
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