Halitosis Clinical Trial
Official title:
Clinical Evaluation of Some Local Antimicrobial Agents' Adjunctive Effects On Periodontal Parameters and Halitosis With Subgingival Ultrasonic Instrumentation in Periodontitis Patients: A Randomized Clinical Study
The aim of this trial was to establish the clinical efficacy of Listerine and chlorhexidine
(CHX) when used as a cooling agent with ultrasonic instrumentation, on periodontal parameters
and halitosis.
Ninety patients with periodontal disease participated for the study. Individuals were
randomly selected to a control and test groups. At baseline, all subjects completed a
questionnaire and carried out an examination. Standard periodontal outcome variables were
assessed. For both groups, the plaque index (PI), gingival index (GI), pocket depth (PD),
bleeding on probing (BOP) and clinical attachment level (CAL) scores were enrolled at
baseline and after 30 days. Volatile sulphur compound (VSC) levels were evaluated by a
Halimeter (Interscan Corp., Chatsworth, CA, USA) at baseline (T0), immediately after
treatment (T1), and at 7 (T2), 14 (T3) and 30 days (T4).
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