Impact of Periodontal Treatment on Serum Levels of Hepcidin and Hemoglobin
Chronic Periodontitis
About this trial
This is an interventional treatment trial for Chronic Periodontitis focused on measuring Chronic periodontitis, Hepcidin, Hemoglobin, Inflammation
Eligibility Criteria
Inclusion Criteria:
- Both sexes
- Aged 30-65 years
- Without other chronic systemic diseases except periodontitis
- At least 20 teeth
Exclusion Criteria:
- Diabetes mellitus
- Congestive heart failure
- Chronic kidney disease
- Malignant neoplasms
- Acquired immunodeficiency syndrome
- Hypertension
- Pregnant women
- Nursing mothers
- Immunosuppressed by medication
- Women with changes in menstrual flow
- Smokers or ex-smokers for less than 10 years
- Usage history of NSAIDs or nonsteroidal and antibiotics within 3 months prior to the study and during the search
- Iron replacement in patients to treat anemia and carrying out subgingival scaling and periodontal surgery in 6 months prior to investigation.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Periodontal Treatment
No Periodontal Treatment
The experimental group underwent nonsurgical periodontal therapy, performed by a single professional who performed the scaling and root planing procedures under local anesthesia using an ultrasonic device and Gracey and mini Gracey curettes, with Robson polishing brush and prophylactic paste. This therapy was performed in two sessions at seven day intervals, with no time limit, according to the needs of each periodontal condition. In each session, subjects received oral hygiene instruction (OHI) for use of toothbrushes for the modified Bass technique, dental floss and other complementary means (interdental brush, single tuft brush, electric toothbrush, etc.) when necessary. Supportive periodontal therapy was performed in 30, 60 and 90 days. Albendazole administration.
Individuals in the control group underwent only the polishing of tooth surfaces with Robson brush and prophylactic paste fine-grained and topical fluoride application. After 90 days, they were reassessed with the same parameters of clinical examination of the baseline.