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Assessment of the Strict Oral Hygiene Phase in the periodontal condition of obese and eutotrophic individuals diagnosed with Periodontitis

Effect of Strict Hygienic Phase prior to Periodontal Therapy on the periodontal and general condition of Obese and Eutrophic patients with Periodontits: Randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5jmx32v
Enrollment
Unknown
Registered
2024-03-11
Start date
2022-04-10
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

periodontitis

Interventions

This is a double-blind randomized clinical trial. Individuals with periodontitis with obesity (n=15) and without obesity (n=15) will be recruited and randomly distributed through software into control

Sponsors

Universidade Federal da Paraíba
Lead Sponsor
Universidade Federal da Paraíba
Collaborator

Eligibility

Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals diagnosed with stage III or IV periodontitis, either eutrophic or with obesity grade I according to the World Health Organization (WHO) criteria; both genders; aged between 30 and 60 years; presence of at least 10 teeth in the oral cavity. These participants should not have a history of systemic disease (HIV, hepatitis), be pregnant or lactating, or have undergone antibiotic therapy in the last three months, periodontal treatment in the last six months, orthodontic appliance use, or be undergoing nutritional therapy

Exclusion criteria

Exclusion criteria: Those affected by Covid-19 during the study period will be excluded; participants who do not complete all data collection assessments; initiate nutritional treatment; who do not follow oral hygiene guidelines during the study period

Design outcomes

Primary

MeasureTime frame
The strict oral hygiene phase prior to periodontitis treatment is capable of causing improvements in inflammation, resulting in a reduction in bleeding, probing depth, improvement in self-perception of halitosis, taste, smell and consequently, nutrition.

Secondary

MeasureTime frame
No secondary outcomes are expected.

Countries

Brazil

Contacts

Public ContactVanessa Alves

Universidade Federal da Paraíba

vanessafalves@hotmail.com+55 (83) 3216-7344

Outcome results

None listed

Source: REBEC (via WHO ICTRP)