Dental intervention i. Full mouth intraoral X-rays (FMX)
ii. Full periodontal exam, diagnosis, Oral hygiene instructions (OHI)
iii. RX: 7 days of p.o. metronidazole (250mg)/amoxicillin (500mg) T.I.D., combined with local chlorhexidine rinses (not for subjects with Kidney transplant).
iv. Single visit intensive scaling and root planning (SRP) (full mouth)
v. Re-evaluation after 4-6 weeks (referral for definitive treatment)
vi. Extraction of teeth deemed hopeless based on periodontal, endodontic or restorative considerations
vii. Caries control, sedative dressing (palliative), referral to endodontic dentist for root canal treatment (RCT)

Chronic Kidney Disease

Chronic Periodontitis, Generalized, Moderate

Dental intervention plan for Group 1 and 3 subjects with periodontitis only, i) Full mouth intraoral X-rays (FMX)
ii. Full periodontal exam, diagnosis, Oral hygiene instructions (OHI)
iii. RX: 7 days of p.o. metronidazole (250mg)/amoxicillin (500mg) T.I.D., combined with local chlorhexidine rinses (not for subjects with Kidney transplant).
iv. Single visit intensive scaling and root planning (SRP) (full mouth)
v. Re-evaluation after 4-6 weeks (referral for definitive treatment)
vi. Extraction of teeth deemed hopeless based on periodontal, endodontic or restorative considerations
vii. Caries control, sedative dressing (palliative), referral to endodontic dentist for root canal treatment (RCT)

dental intervention

Augusta University-Dental College of Georgia

Dental Intervention Plan for Chronic Kidney Disease Patients Awaiting or With Kidney Transplant

The data generate will be published and made available to anyone who requests for samples or data.

Christopher Cutler

Chair and Professor

Augusta University

Periodontal treatment (scaling and root planning) and one tablet containing lactose once a day for three days immediately after the scaling and root planning.

Periodontal treatment (scaling and root planning) and one tablet containing 500 milligrams (mg) of Azithromycin once a day for three days immediately after the scaling and root planning.

Periodontitis

Tablet containing lactose Procedure: Periodontal treatment Scaling and root planning

Lactose tab

Tablet containing 500mg Azithromicyn. Procedure: Periodontal treatment Scaling and root planning

Azithromycin

Universidad Nacional Andres Bello

Efficacy of Azithromycin as an Adjunct to Non-Surgical Periodontal Treatment

Clinical and Microbiological Efficacy of a Azithromycin as an Adjunct to Non-Surgical Periodontal Treatment : A Randomized Controlled Clinical Trial

Before, 1, 3 and 6 month after performing SRP with placebo or azithromycin, PD was measured in all the patients in the study and corresponds to the distance in millimeters from the gingival margin (MG) to the inserted probe´s tip of the most apical portion of the periodontal pocket. It was obtained by measuring with a North Carolina periodontal probe (Hu-Friedy® Manufacturing Inc., Chicago, IL, USA), from the bottom of the pocket to the MG, in a position parallel to the vertical axis of the tooth, with a pressure no greater than 0.25 Newton (N). PD was performed in a circular direction over the entire surface of each tooth, registering the 6 deepest sites per tooth (mesiobuccal, buccal, distobuccal, distolingual, lingual and mesiolingual).
Subsequently, those sites with PD ≥ 3 mm, PD ≥ 4 mm, PD ≥ 7 mm were counted and the student t test was applied to observe if there were significant differences between both treatment groups.

Percentage of subjects presenting low (≤ 4 sites with PD ≥ 5 mm),moderate (5-8 sites with PD ≥ 5 mm) or high (≥ 9 sites with PD ≥5 mm), before and 6 month after performing SRP with placebo or azithromycin.

Before and 6 month after performing SRP, CAL was measured in all the patients in the study and corresponds to the distance measured in millimeters from the cementum enamel junction to the tip of the probe inserted to the most apical portion of the periodontal pocket. It was obtained using a North Carolina periodontal probe (Hu-Friedy® Manufacturing Inc., Chicago, IL, USA), in a position parallel to the vertical axis of the tooth, with a pressure not greater than 0.25 N.

Before,1,3 and 6 month after performing SRP, BI was measured in all the patients in the study. BI is percentage of dental surfaces with staining, through the use of biofilm developers. To obtain the index, a curaprox developer tablet was dissolved in a plastic cup with water and with a cotton ball this solution was applied on all of the tooth surfaces, recording only those that were stained. The calculation was made by dividing the surfaces that stained by the total surfaces, which corresponds to the number of teeth present multiplied by 4, and multiplying this value by 100. Subsequently, student t test was applied to observe if there were significant differences between both treatment groups.

Before,1, 3 and 6 month after performing SRP, BOP was measured in all the patients in the study. BOP is the percentage of surfaces that bleed when probing. It was recorded during PD measurement with a North Carolina periodontal probe (Hu-Friedy® Manufacturing Inc., Chicago, IL, USA) and was considered positive if it occurs 20 seconds after probing. The calculation was made by dividing the sites that bled by the total sites, which corresponds to the number of teeth present multiplied by 6, and multiplying this value by 100. Subsequently, student t test was applied to observe if there were significant differences between both treatment groups.

Before, 3 and 6 month after performing SRP, the microbiological examination was performed on both groups. The biofilm samples were analyzed to detect the presence of four bacterial species: Porphyromonas gingivalis (Pg), Tannerella forsythia (Tf), Treponema denticola (Td), Fusobacterium nucleatum (Fn) by Polymerase chain reaction (PCR).

Mariely Navarrete

Associate Professor, Director of Graduate Periodontics Faculty of Dentistry Andres Bello University, Viña del Mar campus

A double-blind, randomized controlled trial, where patients with a history of Moderate Periodontitis with moderate rate of progression (Stage II grade B) and Severe Periodontitis with potencial for additional tooth loss and moderate rate of progression (Stage III grade B). The intervention group received non-surgical periodontal therapy (SRP) plus azithromycin, and the control group received SRP plus placebo. The clinical variables were measured before the treatment, and in the first, third and sixth month of the end of the SRP, while the microbiological variables were measured before the treatment and in the third and sixth month after treatment.

Procedure: SRP Dietary Supplement: Vitamin D3 Oral supplementation 25000 IU once per week for 6 months Other Name: Cholecalciferol

Procedure: SRP Dietary Supplement: Placebo Oral supplementation once per week for 6 months

Generalized Chronic Periodontitis

Vitamin D Deficiency

Oral supplementation 25000 IU once per week for 6 months

Vitamin D3

Oral supplementation once per week for 6 months

Placebo

Cliniques universitaires Saint-Luc

Effects of Vitamin D Supplementation During a Non-surgical Treatment of Generalized Chronic Periodontitis

Effects of Vitamin D Supplementation During a Non-surgical Treatment of Generalized Chronic Periodontitis: A Randomized Double-blinded Placebo Controlled Clinical Trial

It will be decided at the end of the study

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

All patients were scheduled for open flap debridement surgery on at least two quadrants ≥1 weeks apart.One group will receive Low Dose Diclofenac tablets (25mg Diclofeanc and 325 mg paracetamol), BID for 3 days. The patients who are diagnosed with generalized moderate/severe chronic periodontitis will be included in study. For each quadrant, a flap was raised under local anesthesia (2% lignocaine with 1:80,000 epinephrine). In both the quadrants same technique of anesthesia will be employed. The location and the extent of surgery, volume of the local anesthesia given, and time required to perform the surgical procedure will be recorded in the patient file. Patients will be instructed to complete a pain diary chart for 3 days.

Other group will receive Diclofeanc (50mg Diclofenac and 325mg paracetamol), BID for 3 days. The patients who are diagnosed with generalized moderate/severe chronic periodontitis were included in study. For each quadrant, aperiodontal flap was raised under local anesthesia (2% lignocaine with 1:80,000 epinephrine). In both the quadrants same technique of anesthesia will be employed. The location and the extent of surgery, volume of the local anesthesia given, and time required to perform the surgical procedure was recorded in the patient file. Patients were instructed to complete a pain diary chart for 3 days.

Chronic Periodontitis

it is a split mouth design in which one side recieved low dose diclofenac(25mg) after periodontal flap surgery and in next week second side will recieve diclofenac 50mg after flap surgery.

low dose diclofenac

Dental

To Compare Efficacy of Low Dose Diclofenac (25mg) in Management of Postoperative Pain After Periodontal Flap Surgery

To Compare Efficacy of Low Dose Diclofenac (25mg) in Management of Postoperative Pain After Periodontal Flap Surgery: A Clinical Trail.

it messures pain intensity it is an 10cm line anchored by two extremes 0 for no pain and 10 for extreme pain

periodontitis/nausea

Dental Intervention Plan for Chronic Kidney Disease Patients Awaiting or With Kidney Transplant

Efficacy of Azithromycin as an Adjunct to Non-Surgical Periodontal Treatment

Effects of Vitamin D Supplementation During a Non-surgical Treatment of Generalized Chronic Periodontitis

To Compare Efficacy of Low Dose Diclofenac (25mg) in Management of Postoperative Pain After Periodontal Flap Surgery

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