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Evaluation of the Laser in Periodontal and Bone Healing in Diabetics

Not Applicable
Conditions
Periodontitis
Diabetes Mellitus
Tooth Loss
Registration Number
RBR-223s4bw
Lead Sponsor
niversidade Federal de Uberlândia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Study 1: Participants will be selected according to the following
inclusion criteria: 18 years old, positive diagnosis for Grade B or C periodontal disease, stages 2-4; presence of at least 16 teeth in the oral cavity, with at least 4 non-neighboring sites with a probing depth of 5 mm and bleeding, absence of periodontal treatment one year before the research and not having used antibiotics in the last three months . Study 2: During study 1, patients who consent to participate in study 2 must present the following characteristics: Individuals over 18 years of age; individuals with teeth condemned due to lack of periodontal support; individuals who are indicated for future rehabilitation with an implant (in the region of the units to be extracted); individuals with ASA I or II classification; individuals with the cognitive capacity to maintain their own oral hygiene.”

Exclusion Criteria

"Study 1: The following will be excluded from the study: pregnant or lactating women, who have periodontal treatment in less than a year, who have used antibiotics in the last three
months, patients using antiresorptive medications.Study 2: The following will be excluded from this study: patients who are metabolically decompensated (ASA classification equal to or greater than III - except diabetics); chronic users of antiresorptive and immunosuppressive medications; patients who present acute periodontitis; heavy smokers (more than 10 cigarettes per day); pregnant and breastfeeding women; history of radiotherapy to the head and neck; have a diagnosis of bruxism; immunosuppressed; teeth with root dilaceration or condition that requires odontosection.”

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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