Periodontally healthy Chlorhexidine,
Conditions
Interventions
On Day 1 of each experimental period,
GCF samples were taken from the mesial or distal sites of the first premolar tooth in each quadrant. Full mouth GI was recorded. Professional prophylaxis was then performed to remove all supra-
gingival plaque to establish a baseline of zero plaque scores. The subjects were then asked to stop oral hygiene procedures for the following 4 days. During this period,
the only means of oral hygiene that they were allowed,
was the use of the mouthwash that was allocated to them. Mouthwashes were given in identical opaque bottles. Subjects were asked to rinse with 20 ml of the allocated mouthwash twice daily for 30 secon
once in the morning after breakfast,
once at night before going bed. Subsequent rinsing with water,
drinking or eating were not allowed for 30 min after each rinsing time. Rinsing was performed at home without supervision. All instructions were given in detail verbally as well as in written form. To
subjects were asked to note the time of use of intervention products onto a calendar record chart and asked to return bottles that contain mouthwashes. On Day 5 of each experimental period,
all the measurements including GI and PI and GCF sampling were repeated. Finally,
all subjects received a satisfaction questionnaire (SQ) to evaluate their attitude towards the used product.,On Day 1 of each experimental period,
gingival plaque to establish a baseline of zero plaque scores. The subjects were then asked to stop oral hygiene procedures for the following 4
Active Comparator Device,Experimental Device,Placebo Comparator Device
Chlorhexidine-
containing mouthwash ,Hyaluronic Acid-
containing mouthwash ,Distilled water
Sponsors
NONE
Eligibility
Sex/Gender
All
Age
23 Years to 25 Years
Inclusion criteria
Inclusion criteria: presence of at least 24 natural teeth (excluding third molars), healthy or early gingivitis subjects, no fixed or removable prostheses and orthodontic appliances, no predisposing oral factors causing local irritation and plaque retention, no presence of systemic diseases, no lactation or pregnancy, no history of drug abuse, no medications, no use of systemic or topical oral antimicrobial therapy in the previous 3 months, no current smoker or smoker over the past year.
Exclusion criteria
Exclusion criteria: Periodontally diseased subjects, presence of fixed or removable prostheses and orthodontic appliances, allergic reactions to the used products
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plaque Index Evaluation day 5 Turesky modification of Quigley Hein Index | — |
Secondary
| Measure | Time frame |
|---|---|
| Gingival Index day 0, day 5 Modified Gingival Index | — |
Countries
Turkey
Contacts
Public ContactGizem Ince Kuka
Yeditepe University
Outcome results
None listed