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The effect of antibiotic therapy combined with Gingival Inflammation treatment in individuals with Diabetes

Evaluation of the effectiveness of Antimicrobial Therapy with Amoxicillin and Metronidazole as an adjunct to Periodontal Treatment in individuals with type II Diabetes: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5hq9fst
Enrollment
Unknown
Registered
2025-07-29
Start date
2025-06-01
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, Type 2

Interventions

This is a randomized, double-blind clinical trial aimed at evaluating the effect of adjunctive antimicrobial therapy with amoxicillin and metronidazole to non-surgical periodontal treatment in individ

Sponsors

Universidade Federal De Minas Gerais
Lead Sponsor
Universidade Federal De Minas Gerais
Collaborator

Eligibility

Age
30 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes mellitus and stage II or III periodontitis; patients without diabetes; aged 30 years or older; of both sexes; with a minimum of fourteen teeth; who agree to participate in the research by signing an informed consent form (ICF)

Exclusion criteria

Exclusion criteria: Individuals with diseases that affect the immune system; smokers; pregnant or breastfeeding women; individuals allergic to amoxicillin or metronidazole; individuals who have undergone periodontal treatment in the last 6 months; individuals who have received antimicrobial or anti-inflammatory therapy in the last 3 months; individuals who change their diabetes medication during the study period

Design outcomes

Primary

MeasureTime frame
A reduction in probing depth is expected, verified through manual probing, based on an observed variation of at least 1 mm between pre- and post-intervention measurements.

Secondary

MeasureTime frame
A reduction in the percentage of sites with bleeding on probing is expected, verified through manual probing, based on the observed variation between pre- and post-intervention measurements.

Countries

Brazil

Contacts

Public ContactRafael Lima

Universidade Federal De Minas Gerais

rafaelesteveslima@ufmg.br+55-31-34092427

Outcome results

None listed

Source: REBEC (via WHO ICTRP)