None listed
Conditions
Brief summary
This is a two stage project: (1) Randomized controlled clinical trial to test the null hypothesis that was there is no difference in the clinical efficacy on treatment of plaque-induced gingivitis between nanosilver and chlorhexidine mouthwashes (primary hypothesis) and plaque, gingival and papilla bleeding scores reduction and improvement after two and four weeks from mouth rinsing (secondary hypothesis) followed by (2) Microbiological study to assess antimicrobial efficacy of nanosilver mouthwash and compared with chlorhexidine mouthwash on treatment of plaque-induced gingivitis and to confirm the counting of the bacteria after application of the mouth wash to the patient and taking the plaque sample.
Interventions
This study is a triple-blinded randomized controlled comparative trial of four weeks duration investigating the efficacy of a locally available nanosilver and chlorhexidine mouth wash in the treatment of plaque-induced gingivitis. Subjects received a dental prophylaxis in the past two weeks prior to the baseline examination. Enrolled subjects were then randomly divided into two groups: (1) Control group who rinsed with 0.12% CHX Chlorhexidine Glucognate mouthwash utilizing 10 mL twice daily for one minute. (2) Experimental group who rinsed with less than 0.01% NS Nanosilver mouthwash utilizing 10 mL twice daily for one minute. All patients received a complete dental prophylaxis to remove all plaque, calculus and extrinsic stain before entering the study. The participants were motivated on regular intervals by personal and phone contact to use soft tooth brush, brush only with similar toothpaste (Colgate) and to brush their teeth twice daily, once in the morning after breakfast and once in the evening before bedtime. They were instructed to brush a minimum of 3 minutes to ensure thorough brushing. They also were informed about the same brushing technique (bass technique). They were instructed to rinse their mouth with mouth wash at least half an hour after tooth brushing and instructed not to take any liquid o food for at least 30 minutes. The subjects were instructed not to take any liquid or food into the mouth for at least 30 minutes after using mouth wash to avoid reduction the substantively of mouth wash, thus decreasing the efficacy of the mouth wash and to diminish the side effects of CHX like staining and bad taste. Then we contacted the patients every day at the morning and evening during a period of study by missed calls and message text to remind them. After one week from rinse use the patients returned the empty bottles to receive another one and delivery of the patient diary supplied by the researcher.
Sponsors
Study design
Eligibility
Inclusion criteria
The inclusion criteria of this study comprised good general health, availability for the 4 weeks duration of the study, patients who have evidence of plaque-induced gingivitis without periodontitis, and a minimum of 20 natural teeth, excluded third molars.
Exclusion criteria
Subjects were excluded from the study if they had any of the following conditions: orthodontic bands; partial removable dentures; pregnant or breast feeding women; subjects who had systemic disorders and/or undertake medication which might influence the periodontal; individuals with history of allergic to oral consumer products; smoking; patients who received periodontal treatment or antibiotic therapy any time during the one month prior to entry into the study; subjects who had tumor(s) or significant pathology in the soft or hard tissues of the oral cavity; five or more carious lesions needful immediate care.