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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06204185
Other study ID # FD-ASUREC.IM011967
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2019
Est. completion date November 30, 2022

Study information

Verified date January 2024
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study to evaluate the clinical and biochemical efficacy of 1% Metformin gel in treatment of periodontitis patients


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date November 30, 2022
Est. primary completion date June 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria: - Patients with Stage III Grade A Periodontitis. - Systemically free according to the modified Burkitt's health history questionnaire, Group I. (Glick et al., 2021). - Good compliance with the plaque control instructions following initial therapy. - Availability for follow up and maintenance program. Exclusion Criteria: - Smokers - Pregnant and lactating females. - Vulnerable groups of patients' e.g (prisoners, handicapped patients and decisionally impaired individuals).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Metformin
Locally delivered Metformin gel in the treatment of periodontitis patients
Placebo
Placebo gel consist of drug without the active component.

Locations

Country Name City State
Egypt Sameh Magdy Abou El-Kheir Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary RANKL and Osteoprotegrin levels in Gingival Crevicular Fluid before & after application of metformin as an adjunctive therapy to non surgical periodontal treatment of Stage III periodontitis. Baseline and 1 month after the gel application
Secondary Plaque index (PI) Baseline, 3 Months and 6 Months post operatively.
Secondary Gingival Index (GI) Baseline, 3 Months and 6 Months post operatively.
Secondary Probing depth (PD) Baseline, 3 Months and 6 Months post operatively.
Secondary Clinical attachment level (CAL) Baseline, 3 Months and 6 Months post operatively.
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