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Local effect of Metformin gel 1% in Periodontal treatment of patients with Type II Diabetes Mellitus and Periodontitis

Metformin gel in the Periodontal treatment of patients people with type II Diabetes Mellitus with Periodontitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
REBEC
Registry ID
RBR-2c3t8gb
Enrollment
Unknown
Registered
2023-11-02
Start date
2022-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes mellitus

Interventions

This is a randomized, double-blind clinical study. A total of 39 people meeting the eligibility criteria were randomly assigned to two groups. Both the researchers who evaluated the outcomes and the p
E06.470

Sponsors

Centro de Ciências Biológicas e da Saúde CCBS - Universidade Estadual do Oeste do Paraná
Lead Sponsor
Centro de Ciências Biológicas e da Saúde CCBS - Universidade Estadual do Oeste do Paraná
Collaborator

Eligibility

Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients of both sexes with Periodontitis stages 1, 2, 3 or 4, grade B or C, presenting bleeding on probing and gingival inflammation. Patients must have the pathophysiological condition of Type II Diabetes Mellitus (diagnosed by endocrinologists) and use systemic Metformin. Patients who agree to participate in the study, signing the informed consent form. Patient aged between 18 and 70 years

Exclusion criteria

Exclusion criteria: Patients with a positive history in the last 6 months of broad-spectrum antibiotic therapy, steroidal anti-inflammatory drugs or immunosuppressive therapy in the 3 months prior to the study. Pregnant or lactating. History of periodontal treatment in the last 6 months. Smoking or quitting the habit for less than 5 months. Patients who have less than 4 teeth or have misaligned teeth in the dental arch. Patient under 18 years old or over 70 years old

Design outcomes

Primary

MeasureTime frame
Expected Outcome 1: It is expected to improve the clinical parameters of clinical probing depth and clinical attachment level, decrease the amount of interleukin-17 present in the crevicular fluid.

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactBruna Ferreira

Universidade Estadual do Oeste do Paraná

bruna-sad@hotmail.com+55(45)3220-3000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)