A clinical trial to study the effect of Gluma and Er,Cr:YSGG Laser in patients with tooth hypersensitivity
- Registration Number
- CTRI/2024/03/064425
- Lead Sponsor
- Dr. Sagarika Sortey
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Premolar with Class 3 Non-Carious Cervical Lesion showing hypersensitivity.
Patient showing willingness to participate in the study for 1 month.
i. Carious lesion on the selected or neighbouring tooth.
ii. Restorations on the selected tooth.
iii. Any desensitizing therapy on the selected tooth during the last 6 months
iv. Periodontal surgery within last 3 months
v. Nonvital tooth, cracked tooth syndrome
vi. Tender tooth in the same quadrant as the hypersensitive teeth.
vii. Patients undergoing orthodontic treatment
viii. Pregnant/lactating females.
ix. Smokers, alcoholics.
x. Patients taking antibiotics/analgesics/anti-inflammatory/anti-depressive drugs, patients having cognitive dysfunctions/general communication difficulties.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To assess the hypersensitivity in Non-Carious Cervical Lesions (NCCLs). <br/ ><br>2)To assess the effect in hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin after pre-treatment with Gluma and Er,Cr:YSGG laser vs without pre-treatment. <br/ ><br>3)To compare the efficacy of Gluma and Er,Cr:YSGG laser in reducing hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin vs without pre-treatment. <br/ ><br>Timepoint: VAS scale will be used to measure the pain response before treatment 24hrs post restoration 15 days and 1 month. <br/ ><br>
- Secondary Outcome Measures
Name Time Method no secondary outcomeTimepoint: nil