Metronidazole vs Azithromycin in Periodontal Surgery for Patients Positive to Porphyromonas Gingivalis

Surgery Clinical Trial

Official title:

Clinical and Microbiological Comparison of Two Different Systemic Antimicrobials (Azithromycin Versus Metronidazole) as Adjuncts to Periodontal Surgery in the Treatment of P.Gingivalis Periodontitis Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03862456
• Other study ID #: ATB1
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 2013
• Est. completion date: July 2019

Study information

• Verified date: February 2019
• Source: Universidad Complutense de Madrid
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to determine whether, in patients with non treated periodontitis (stage III and IV) positive to Porphyromonas gingivalis, the use of systemic antimicrobials (metronidazole versus azithromycin) as an adjunctive treatment to periodontal surgery provides clinical and microbiological benefits.

Description:

Design: randomized, parallel and triple blind clinical trial

Sample: Patients with periodontitis (stages III and IV) and positive to Porphyromonas gingivalis who potentially need periodontal surgery were recruited. 25 patients were randomized to the test group (periodontal surgery + azithromycin) and another 25 subjects to the control group (periodontal surgery + metronidazole).

Study visits:

• Examiner calibration

• Recruitment of patients. Screening. Data collection (clinical and microbiological variables).

• Phase I.

• Non-surgical periodontal treatment (2 visits).

• Reevaluation at 6 weeks. Data collection (clinical and microbiological variables). Identification of study candidate patients (Patients with probing pocket depth > 5 mm and positive to Porphyromonas gingivalis). Randomization of study groups.

• Phase II. Surgical periodontal treatment.

• Periodontal surgery sessions. In the last surgery, the antibiotic test (azithromycin) or metronidazole (control) is administered according to randomization.

• Suture removal 1 week after performing periodontal surgery. Data collection 1 week after antibiotic consumption with the last surgery (patient-centered variables on the side effects of antibiotics).

• Re-evaluation of the surgical phase at 6 weeks after the last surgery session. Data collection (clinical variables).

• Phase III. Periodontal maintenance.

• Maintenance 1 (3 months post surgery). Data collection (Clinical and microbiological variables).

• Maintenance 2 (6 months post surgery). Data collection (Clinical and microbiological variables).

• Maintenance 3 (9 months post surgery). Data collection (Clinical variables).

• Maintenance 4 (12 months post surgery). Data collection (Clinical and microbiological variables).

• Maintenance 5 (4 years post surgery). Data collection (Clinical and microbiological variables).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 50
• Est. completion date: July 2019
• Est. primary completion date: July 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Diagnosis of periodontitis (stages III or IV) that may require periodontal surgery

• Have at least 10 teeth in function, excluding third molars.

• Present locations with probing depth (PS)> 6 mm in at least 30% of the teeth.

• Present radiographic evidence of moderate-severe bone loss in at least 30% of the dentition.

• Detection of P. gingivalis in subgingival samples taken at the screening visit as well as in the post-scaling and root planning visit and processed by culture.

• Systemically healthy patients.

Exclusion Criteria:

• Pregnant or lactating women.

• Presenting systemic pathology and / or taking medication that may affect the periodontal situation and / or patients requiring antibiotic prophylaxis.

• Have received systemic antimicrobial treatment in the previous 6 months.

• Have received periodontal treatment in the 6 months prior to the beginning of the study.

• Patients allergic to metronidazole, or to any of the components of commercial formulations thereof (Flagyl®).

• Patients allergic to azithromycin, or to any of the components of commercial formulations thereof (Zithromax®).

• Patients who refuse to sign the informed consent.

Related Conditions & MeSH terms

• Periodontitis
• Surgery

Intervention

Other:
• Azithromycin
azithromycin (500 mg/24h/3 days)
• Metronidazole
metronidazole (500 mg/8h/7 days)

Locations

Country	Name	City	State
Spain	Faculty of Dentistry, Univesity Complutense, Madrid	Madrid

Sponsors (1)

Lead Sponsor	Collaborator
Universidad Complutense de Madrid

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Probing pocket depth (PPD)	Full mouth measurement at 6 sites per tooth, with a manual periodontal probe University North Carolina 15 (UNC-15 mm)	At 6 weeks after periodontal surgery
Secondary	Probing pocket depth (PPD)	Full mouth measurement at 6 sites per tooth, with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Gingival Recession (REC)	Full mouth measurement at 6 sites per tooth, with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Plaque index (PlI)	Full mouth measurement at 6 sites per tooth, with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Gingival index (GI)	Full mouth measurement of the bleeding on probing at 6 sites per tooth, with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Furcations	Measurement of furcations with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Clinical attachment level (CAL)	Full mouth measurement at 6 sites per tooth, with a manual periodontal probe UNC-15 mm	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I), 6 weeks after the last surgery session (Reevaluation Phase II) and during the maintenance Phase III (3, 6, 9, 12 and 48 months after periodontal surgery)
Secondary	Total bacterial counts	A microbiological sample is taken with sterilized paper points from the gingival crevicular fluid and the total bacterial counts (expressed in total colony-forming units) are analyzed by culture.	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I) and during the maintenance Phase III (3, 6, 12 and 48 months after periodontal surgery)
Secondary	Percentage of periodontal pathogens	Determination of the percentage of the following periodontal pathogens: Porphyromonas gingivalis; Tannerella forsythia; Aggregatibacter actinomycetemcomitans; Prevotella intermedia; Fusobacterium nucleatum; Eikenella corrodens; Campylobacter rectus; Capnocytophaga sp.; Enterobacter sp.	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I) and during the maintenance Phase III (3, 6, 12 and 48 months after periodontal surgery)
Secondary	Counts of periodontal pathogens	Determination of the following periodontal pathogens: Porphyromonas gingivalis; Tannerella forsythia; Aggregatibacter actinomycetemcomitans; Prevotella intermedia; Fusobacterium nucleatum; Eikenella corrodens; Campylobacter rectus; Capnocytophaga sp.; Enterobacter sp.	At the beginning of the study, 6 weeks after scaling and root planning (Reevaluation phase I) and during the maintenance Phase III (3, 6, 12 and 48 months after periodontal surgery)
Secondary	Appearance of side effects after taking antibiotic	The patient was asked if he had side effects after taking antibiotic (Yes / No)	1 week after antibiotic consumption
Secondary	Type of adverse effect after taking antibiotic	The patient was asked to write freely on a form the type of side effect suffered	1 week after antibiotic consumption
Secondary	Degree of affectation	The patient was asked to categorize the degree of affectation (mild, moderate or severe) of the secondary effect of the antibiotic if it had appeared.	1 week after antibiotic consumption