Investigation of the efficacy of desensitizing effects of bioactive glass-incorporated universal dentin adhesives: a split-mouth model clinical trial
- Conditions
- Diseases of the digestive system
- Registration Number
- KCT0008101
- Lead Sponsor
- Kyung Hee University Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
The selection criteria are as follows.
(1) Adult men and women over the age of 19 with permanent teeth
(2) Those who meet the criteria 1 or 2 of the American Society of Anesthesiologists (ASA)
(3) Those who have consented to participate in the clinical trial and voluntarily consented in writing
(4) Subjects with exposed root surfaces showing hypersensitivity to 50g force probing and air test through clinical examination or teeth showing cervical abrasion exist in two or more quadrants
- The tooth must be free from lesions such as dental caries, defective restorations, or fractured teeth.
- The tooth must have no apical lesions.
- The tooth must not have received any treatment that may cause postoperative hypersensitivity, such as restoration, periodontal surgery, orthodontic treatment, within 3 months.
The exclusion criteria are as follows.
(1) Persons with a history of hypersensitivity to quasi-drugs for clinical trials or drugs of the same class
(2) Those who received hypersensitivity treatment within 3 months from the date of participation in the clinical trial
(3) Those who regularly take antibiotics and painkillers due to medical history
(4) Pregnant and lactating women
(5) those with a disease that can increase the acidity of the oral cavity; Anorexia, reflux esophagitis, etc.
(6) Consuming excessively acidic foods or beverages; Lemon or tomato more than 2 times/day, acidic beverage (sports drink, energy drink, fruit juice) more than 1L/day
(7) Those who have difficulty in reading and understanding the instructions provided by clinical research
(8) Persons judged to be inappropriate to participate in clinical trials by other investigators
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Schiff cold air sensitivity scale
- Secondary Outcome Measures
Name Time Method visual analog scale