Unique ID issued by UMIN | UMIN000007384 |
---|---|
Receipt number | R000008702 |
Scientific Title | A randomized controlled clinical trial to examine the microbiological and clinical effects of oral antimicrobials on patients with periodontitis receiving supportive periodontal therapy |
Date of disclosure of the study information | 2012/03/10 |
Last modified on | 2016/03/27 11:44:42 |
A randomized controlled clinical trial to examine the microbiological and clinical effects of oral antimicrobials on patients with periodontitis receiving supportive periodontal therapy
A clinical trial to examine the effects of oral antimicrobials on patients with periodontitis in SPT phase
A randomized controlled clinical trial to examine the microbiological and clinical effects of oral antimicrobials on patients with periodontitis receiving supportive periodontal therapy
A clinical trial to examine the effects of oral antimicrobials on patients with periodontitis in SPT phase
Japan |
Moderate to severe periodontitis
Dental medicine |
Others
NO
To examine the effects of 2 different oral antimicrobials on microbiological and clinical parameters in patients with periodontitis in SPT phase.
Efficacy
The number of total bacteria and some periodontopathic bacteria in subgingival plaque
Probing pocket depth(PD)
Bleeding on probing(BOP)
Antibody levels in serum against periodontopathic bacteria Concentration of the drugs in gingival crevicular fluid
Interventional
Parallel
Randomized
Open -but assessor(s) are blinded
Active
2
Treatment
Medicine |
Test group
1. 25 patients
2. Patients take 500mg of test drug per day, once a day for 3 days
Control group
1. 25 patients.
2. Patients take 200mg of sitafloxacin hydrate (Gracevit) per day for 5 days.
20 | years-old | <= |
Not applicable |
Male and Female
1. 20 years or older persons who obtained written informed consent.
2. Persons who have diagnosed as moderate to severe chronic or aggressive periodontitis.
3. Persons who have completed active periodontal treatment and received SPT.
4. Persons who have more than 15 teeth.
5. Persons who have more than 2 teeth with PD more than 5mm and BOP (+)
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.
50
1st name | |
Middle name | |
Last name | Kazuhisa Yamazaki |
Niigata University
Graduate school of medical and oral sciences,
2-5274, Gakkocho-dori, Chuo-ku, Niigata, 951-8514, Japan
025-227-6161
kaz@dent.niigata-u.ac.jp
1st name | |
Middle name | |
Last name | Takako Nakajima |
Niigata University
Medical and dental hospital,
2-5274, Gakkocho-dori, Chuo-ku, Niigata, 951-8514, Japan
025-227-6161
takako@dent.niigata-u.ac.jp
Niigata University Medical and Dental Hospital
Daiichi-Sankyo Co., LTD
Profit organization
NO
2012 | Year | 03 | Month | 10 | Day |
Published
http://aac.asm.org/content/early/2016/01/04/AAC.02575-15.abstract
Completed
2011 | Year | 09 | Month | 28 | Day |
2011 | Year | 11 | Month | 01 | Day |
2014 | Year | 11 | Month | 30 | Day |
2014 | Year | 12 | Month | 31 | Day |
2015 | Year | 02 | Month | 28 | Day |
2015 | Year | 02 | Month | 28 | Day |
2012 | Year | 02 | Month | 27 | Day |
2016 | Year | 03 | Month | 27 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008702