A randomized controlled clinical trial to examine the microbiological and clinical effects of oral antimicrobials on patients with periodontitis receiving supportive periodontal therapy
Not Applicable
- Conditions
- Moderate to severe periodontitis
- Registration Number
- JPRN-UMIN000007384
- Lead Sponsor
- iigata University Medical and Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1. Persons who received debridement in periodontal pockets for the past one month prior to this study. 2. Persons who received SRP with local anesthesia for the past three month prior to this study. 3. Persons who took antimicrobials (except external use) for the past three month prior to this study. 4. Persons who have the medical history of hypersensitivity to new quinolone or macrolide antimicrobials. 5. Persons who are pregnant or suspected to be pregnant. 6. Persons who have severe diabetes, heart diseases, or dysfunction of kidney or liver. 7. Persons who are judged to be unqualified for this study subjects by investigators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method