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Charles Foster
Charles Foster

Where To Buy Perio Plus Oral Rinse !!EXCLUSIVE!!


CHX is an effective and broad-spectrum biocide, antiseptic and disinfectant agent that combats a wide range of gram-negative and gram-positive bacteria, yeasts, fungi, and many other kinds of microorganisms. The beneficial effects of CHX are confirmed as having a significant effect on dental plaque formation and accumulation, and therefore are used in prophylaxis and treatment of dental caries, gingivitis and periodontitis. There are various concentrations of this formula in many specialised oral care products, suitable for both short- and long-term use.




where to buy perio plus oral rinse



The results have shown that Perio plus CHX formulations were effective against the selected oral bacteria responsible for biofilm masses that are known to cause periodontal disease. The most important finding is that even the low-concentration CHX formulations with additives slowed down cariogenic biofilm formation to a greater extent than additive-free solutions with the same or even higher concentration of CHX.


The findings of the study demonstrated that the unique formula of Perio plus is clinically proven to be more effective than CHX alone in means of limiting the formation of oral biofilm. Overall, the activity of the these advanced CHX formulations and solutions was highly effective in the case of reducing biofilm formation, but less so on periodontal biofilm that has already formed.


Therefore, it is important to emphasise the importance of proper mechanical removal of biofilm by scaling and root planing in the initial therapy of periodontitis. For more-effective home treatment, these procedures can be followed with the application of tested Perio plus CHX and Citrox formulas, since it has been clinically proven that they are beneficial in the fight against oral microorganisms that cause many common dental diseases.


Chlorhexidine oral rinse should be used after you have brushed and flossed your teeth. Rinse the toothpaste completely from your mouth with water before using the oral rinse. Do not eat or drink for several hours after using the oral rinse.


Chlorhexidine may change the way foods taste to you. Sometimes this effect may last up to 4 hours after you use the oral rinse. In most cases, this effect will become less noticeable as you continue to use the medicine. When you stop using chlorhexidine, your taste should return to normal.


Off-label uses of chlorhexidine are where many of the serious issues originate. It was not created to be used with implants, periodontal therapy, or oral surgery. The Food and Drug Administration has reported more than 52 cases of anaphylaxis between 1998 and 2010, and this number has been increasing.5 The serious cases involving allergic reactions reported outcomes that required emergency department visits or hospitalizations to receive drug and other medical treatments. Two of these cases actually resulted in death. In both scenarios, each patient had left the dental office after an extraction with instructions to use chlorhexidine rinse at home. As previously mentioned, it takes 1,200 ppm of chlorhexidine to achieve results.2 For this reason, it should not be used with open wounds. In the cases in which patients died, both had open wounds and the uptake of the active ingredient was too high, inducing severe allergic reactions.5


Citrox naturally enhances the effects of chlorhexidine to create a high-performance mouth rinse that protects the oral cavity, with minimal risk of irritation, discolouration and disruption to taste.


We are happy to present you a new, enhanced version of the #1 high strength sodium fluoride home-care rinse recommended by Canadian dental professionals: X-PUR Opti-Rinse Plus.Patented and Unique FormulationX-PUR Opti-Rinse Plus unique formulation includes Citrox, which is a natural bioflavonoid complex. Apart from being all-natural, organic and hypoallergenic, Citrox is very effective at killing bacteria and viruses at very low concentrations. It is a unique plant-based and patented antimicrobial bioflavonoid complex offering a powerful antimicrobial, antioxidant, antifungal, antiviral and anti-inflammatory effect. Citrox is biodegradable, safe to handle, eco-friendly, alcohol-free, does not contain synthetic fragrances or colourants, and is also free of GMO, petrochemicals and allergenic substances.Health Canada Indication: Helps Prevent Plaque & GingivitisX-PUR Opti-Rinse Plus is not only a solution in your caries management protocol, but also for your periodontal patients. Tackling gingivitis in a profond way!A Larger Bottle for the Same PriceThe second enhancement includes an increase in the bottle size. The X-PUR Opti-Rinse Plus now comes in a 500ml bottle compared to a 473ml one, and for the same price!A New Mint Flavour for the 0.05% ConcentrationX-PUR Opti-Rinse Plus will now be offered in a delicious mint flavour specifically designed for the particular taste of adult patients.


Layout table for study information Study Type : Interventional (Clinical Trial) ActualEnrollment : 33 participants Allocation: Randomized Intervention Model: Parallel Assignment Intervention Model Description: Single-centre randomized, parallel design, clinical trial with a 2 week follow-up Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) Masking Description: After surgery, patients will be randomly assigned to study groups corresponding to mouth rinse prescription. The mouth rinse will be assigned by an experimenter not involved in the following steps of the study, in order to maintain the examiner blind. The patient will receive a non-labelled mouth rinse to avoid biases both of the examiner and the patient Primary Purpose: Supportive Care Official Title: Evaluation of the Rinse With Chlorhexidine Plus Hyaluronic Acid Mouthwash in Periodontal Surgical Wound Healing Actual Study Start Date : January 2016 Actual Primary Completion Date : December 2018 Actual Study Completion Date : March 2020 Resource links provided by the National Library of Medicine MedlinePlus related topics: Wounds and Injuries Drug Information available for: Chlorhexidine Chlorhexidine acetate Chlorhexidine hydrochloride Chlorhexidine gluconate Hibiclens U.S. FDA Resources Arms and Interventions Go to Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information Arm Intervention/treatment Experimental: Test group 1administration of a hyaluronic and 0.2% chlorhexidine mouth rinse Procedure: Periodontal surgerySurgery will be performed following a standardized protocol by a single operator (FG). The procedure consists in the performance of a primary full-thickness flap incision, and of a secondary releasing vertical incision of maximum 3 mm limited to keratinized gingiva. At the end of the surgical procedure, soft tissues will be repositioned by means of a suture involving only the primary incision, while it will not be performed on the releasing incision. Device: Hyaluronic and 0.2% chlorhexidine mouth rinseThe mouth rinse protocol assigned to each study participant included a 10 ml-rinse for 60 seconds twice-a-day (every 12 hours) for 14 days. Experimental: Test group 2administration of chlorhexidine 0.2% mouth rinse Procedure: Periodontal surgerySurgery will be performed following a standardized protocol by a single operator (FG). The procedure consists in the performance of a primary full-thickness flap incision, and of a secondary releasing vertical incision of maximum 3 mm limited to keratinized gingiva. At the end of the surgical procedure, soft tissues will be repositioned by means of a suture involving only the primary incision, while it will not be performed on the releasing incision. Device: Chlorhexidine 0.2% mouth rinseThe mouth rinse protocol assigned to each study participant included a 10 ml-rinse for 60 seconds twice-a-day (every 12 hours) for 14 days. Active Comparator: Control GroupNo administration of mouth rinses after surgery Procedure: Periodontal surgerySurgery will be performed following a standardized protocol by a single operator (FG). The procedure consists in the performance of a primary full-thickness flap incision, and of a secondary releasing vertical incision of maximum 3 mm limited to keratinized gingiva. At the end of the surgical procedure, soft tissues will be repositioned by means of a suture involving only the primary incision, while it will not be performed on the releasing incision. Outcome Measures Go to Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information Primary Outcome Measures : Pocket probing depth (PPD) [ Time Frame: Measured at Baseline and at day 3, day 7, and day 14 ]Changes in PPD, measured orally through clinical examination. Unit of measure: mm Secondary Outcome Measures : Clinical attachment level (CAL) [ Time Frame: Measured at Baseline and at day 3, day 7, and day 14 ]Changes in CAL , measured orally through clinical examination. Unit of measure: mm Recession of the gingival margin (REC) [ Time Frame: Measured at Baseline and at day 3, day 7, and day 14 ]Changes in REC, measured orally through clinical examination. Unit of measure: mm Bleeding on probing (BOP) [ Time Frame: Measured at Baseline ]BOP, measured orally through clinical examination. Unit of measure: % Angulated bleeding index (AngBI) [ Time Frame: Measured at day 3, day 7, and day 14 ]AngBI, measured orally through clinical examination. Unit of measure: % Plaque index (PI) [ Time Frame: Measured at Baseline and at day 3, day 7, and day 14 ]Changes in PI, measured orally through clinical examination. Unit of measure: % Periodontal Wound Healing Index (PWHI) (Wachtel classification) [ Time Frame: Measured at day 3, day 7, and day 14 ]Changes in PWHI, measured orally through clinical examination on all the incisions, assigning a score from 1 to 5. 041b061a72


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