A Clinical and Imaging Study to Evaluate a Novel Dentifrice
a study on Complication of Personal Oral Hygiene
There is a need for toothpastes that more effectively remove oral biofilm, and inhibit biofilm re-formation. This is particularly important for patients with long-term orthodontic fixtures or prosthodontic appliances, and also for debilitated, diabetic and immunocompromised patients. The objective of this study is to evaluate the effects of toothpastes on plaque presence and removal, dental hard tissue mineralization, erosion, abrasion and microstructure as well as gingival and periodontal health and dry/sore mouth. In addition to clinical scoring and photographs, measurements of tooth and gum sensitivity, saliva volume, pH and buffering, variables may be evaluated using tooth samples worn on removable dental retainers. These samples will be examined outside of the mouth using advanced optical techniques such as Optical Coherence Tomography (OCT), Fluorescence, various forms of microscopy and spectroscopy.
The objective of this study is to evaluate the effects of a novel dental gel, on de- and re-mineralization and the microstructure of the enamel surface in vivo of teeth and on the gingival soft tissue. The purpose of this study is to evaluate the effects of over-the-counter toothpaste Colgate product, Crest Cavity Protection toothpaste and Zendium Classic toothpaste and use imaging devices call Optical Coherence Tomography and Multiphoton Microscopy to measure the change in oral tissue.
Imaging devices are:
- Optical Coherence Tomography, this imaging device can be used to identify the presence of the inflammation of the gum. The inflammation presence in the gingival pockets and compare to the effect of the toothpaste.
- Multiphoton Microscopy, this imaging device can be used to identify the presence of the bacterial. The results can determine effects of the toothpaste on the development and breakup of bacterial and any other changes.
In the first part of this study, 15 subjects moderate gingival inflammation (Löe and Silness Gingival Index ≥2) and pocket depths <4 will be randomly assigned to brush twice daily for 21 days with the test or the control dental gel. On Days 0, 7, 14 and 21, plaque levels (Quigley-Hein, Turesky Modification Plaque Index), gingival inflammation (Löe and Silness Gingival Index) and gingival bleeding (modified Sulcus Bleeding Index) will be determined by one blinded, investigator (Dr. Wilder-Smith) using a pressure sensitive probe. In vivo Optical Coherence Tomography (OCT) and Multiphoton Microscopy (MPM) will be used for in situ imaging. The results from this study will help evaluate the effects of the test dentifrice formulation on plaque removal and maintaining gingival health.
In the second part of this study, in 15 subjects, plaque formation and removal will be quantified using ex vivo Optical Coherence Tomography (OCT) and Multiphoton Microscopy (MPM) imaging of small enamel chips mounted on a simple intra-oral retainer. In this cross over design study the subjects will attend the test site on 11 occasions over an 11 week period. Subjects will have an intra oral retainer manufactured which will be worn for a minimum of 22 hours per day and will have up to 8 sterile human enamel inserts fitted.
The second part of the study will be conducted in three legs with a maximum of 44h of retainer wear each, and each leg will follow the same procedure. 2 different over-the-counter toothpastes and a water control will be used for each leg of the study respectively. There will be a minimum of two weeks between each leg.
The third part of this study will involve 5 subjects with no specific oral health issues. The protocol will involve 3 subjects wearing simple retainers for 3 periods of 2 weeks each with 5 sterilized UCI IRB Approved: 07-22-2016 | MOD# 18976 | HS# 2013-9778 1 of 32 enamel chips attached in the palate area. The study will have 3 legs using a control and 2 active toothpastes. There will be washout of 1-2 weeks between each leg. (Section 3 has been completed as of July 11, 2016)
The fourth part of this study will involve 5 subjects with xerostomia. Subjects will wear simple removable retainers for 2 periods of 1 week each, with 5 sterilized demineralized enamel chips attached in the palate area Fresh enamel chips will be used for each leg of the study. After study completion, chips will be used for Scanning Electron microscopy (SEM) and microhardness measurement. We will provide custom retainers made from impressions of each subject. Upon conclusion of the study, we will analyze the effects of Livionex or Xylimelts use on surface enamel using SEM and microhardness data.
Complication of Personal Oral HygieneOral Hygiene
You can join if…
Open to people ages 18 years and up
- Male or female over the age of 18 of all ages.
- Have a previously diagnosed condition of gingivitis including gingival bleeding and plaque.
- Not pregnant or not lactating.
You CAN'T join if...
- Participated in other clinical study within the last 30 days.
- Plan to receive dental treatment during the study dates.
- History of significant adverse effects following use of oral hygiene products such as toothpastes and mouth rinses.
- Have allergies to personal care/consumer products or their ingredients.
- Have less than 20 teeth (excluding third molars).
- Have been diagnosis with active acquired immunodeficiency syndrome (AIDS) or Hepatitis B/C and other significant disease or disorders.
- Have a history of herpetic infection, recurrent apthous ulcer, or other ulcer forming diseases, abscesses, granulomas, or severe gingivitis.
- Have a history of or are currently taking immunosuppression.
- Have a history of taken antibiotics in the previous 3 months.
- Beckmam Laser Instituteaccepting new patients
Lead Scientist at UC Irvine
- accepting new patients
- Start Date
- Completion Date
- University of California, Irvine
- Study Type
- Last Updated
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