Periodontal Diseases Clinical Trial
Official title:
A Comparison of Mouth Rinse Containing Alcohol-free Chlorhexidine With a Cetylpyridinium Chloride in Periodontal Diseases (A Randomized, Double-blind Clinical Trials)
Aim: clinical effectiveness of 0.05% cetylpyridinium chloride mouth rinse in patients with
gingivitis as compared to non-alcoholic chlorhexidine mouth wash.
Methods & Material: Twenty-four subjects, without systemic diseases, with plaque-induced
gingivitis will be selected for this study. The patients were treated with scaling and root
planing at the baseline; Oral hygiene instructions were given that included brushing twice-
daily, The volunteers brushed their teeth with the Bass brushing technique for at least 2
minutes, these patients were randomly ,equally divided into two groups, Group A: perform
daily mouthwashes twice a day with the solution containing 10 ml of 0.05 cetyl pyridinium,
(Vi-one, Rojin, Cosmetic-Lab, Kurdistan -Iran), Group B: use daily mouthwashes twice a day
with 10ml of the chlorhexidine(Kin Laboratories, Spain), On day 0,7,15 and day 21 of each
phase the Plaque Index (PI), Pocket depth(PD), Stain Index(SI) and Bleeding Index (BI) of
each volunteer were measured.
Status | Completed |
Enrollment | 34 |
Est. completion date | June 2015 |
Est. primary completion date | April 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 34 Years |
Eligibility |
Inclusion Criteria:Inclusion criteria: adult patients with gingivitis, older than 18 years
old, systemically healthy, and having at least 20 teeth. Exclusion Criteria:patients with cavitated caries, no periodontal pockets larger than 4 mm, orthodontic appliances or removable prostheses, allergies to cetyl pyridinium or CHX, use of antibiotics and anti-inflammatory drugs in the past 3 months that might alter normal gingival health, oral prophylaxis outside of study; use of oral chlorhexidine products or participation in an oral rinse study within 3 months prior to baseline examination, pregnancy or nursing, smoking. Study Population 34 eligibles were enrolled in the study, was designed as a Randomized, Double-blind clinical trials. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Islamic Azad University, Tehran |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction of bleeding on probing | Periodontal pobe | 7 days | Yes |
Secondary | Reduction of plaque index | Plaque Index (O'Leary) | 7 days | Yes |
Secondary | Reduction of pocket depth | Periodontal pobe | 7days | Yes |
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