Status:
COMPLETED
Efficacy of INERSAN in Patients With Chronic Periodontitis as Adjunctive to Full Mouth Disinfection
Lead Sponsor:
University of L'Aquila
Conditions:
Chronic Periodontitis
Eligibility:
All Genders
21-70 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate beneficial effects of probiotic Lactobacillus brevis CD2 tablets in addition to the primary treatment for patients with chronic periodontitis (Full Mouth Disin...
Detailed Description
This study will be conducted as a double blind, randomized, parallel group, placebo controlled clinical trial, involving subjects of 21 years of age or older to evaluate the beneficial effects of INER...
Eligibility Criteria
Inclusion
- Patients between 21-70 years of age groups;
- patients with chronic periodontitis in need of primary treatment;
- patients with at least 20 fully erupted teeth;
- patients ready to give written informed consent for participating in the trial;
- patients agreeing to comply with the study protocol and instructions.
Exclusion
- Pregnant women and lactating mothers;
- patients with debilitating systemic diseases;
- patients in needs for prophylactic antibiotics;
- patients treated with antibiotics within 30 days prior to enrollment into the study;
- patients already participant any other clinical trial or participant other investigational drug, or food supplement, in the last 30 days;
- patient having active periapical abscess or periodontal abscess or a history of acute necrotizing ulcerative gingivitis;
- patients not willing to participate in the trial.
- patients with psychiatric problems.
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2015
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT01438333
Start Date
September 1 2011
End Date
March 1 2015
Last Update
June 17 2015
Active Locations (1)
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1
University of L'Aquila, Division of Periodontology
L’Aquila, AQ, Italy, 67100