Status:
COMPLETED
Treatment of Hypersensitivity Using Diode Laser and Desensitising Agent on Fluorosed and Non-fluorosed Teeth
Lead Sponsor:
Krishnadevaraya College of Dental Sciences & Hospital
Conditions:
Fluorosis, Dental
Non-Fluoride Enamel Opacities
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
The present study was designed as a randomised controlled clinical trial which was unicenter, double-blinded, parallel designed study, according to the Consolidated Standards of Reporting Trials (CONS...
Detailed Description
90 Patients visiting the Out Patient of Department of Periodontology, Krishnadevaraya College of Dental Sciences and Hospital, Bengaluru, India, presenting with a chief complaint of dentinal hypersens...
Eligibility Criteria
Inclusion
- • Patients with a positive response for hypersensitivity testing (Pashley, 1990) i.e. cold water testing using ice cold water (Trowbridge et al., 1980),
- Air blow test (Coleman and Kinderknecht, 2000),
- Electric tactile stimulation test (Camps and Pashley, 2003),
- Patients presenting with non-carious cervical lesions in the enamel (Loomba et al., 2013), fluorosed teeth wherein fluorotic enamel staining confirmed by clinical examination, healthy non fluorosed teeth, which was confirmed by clinical examination (Dean, 1934).
Exclusion
- The following were set as the exclusion criteria;
- Patients undergoing any form of restorative endodontic,
- Orthodontic treatment or crown restorations,
- Local defects including caries and fractures,
- Presence of any systemic diseases,
- Acute pain conditions (like apical periodontitis, periapical abscess),
- Presence of periodontal disease or a history of periodontal treatment in last 6 months,
- Usage of desensitising toothpaste or mouth rinse in the last 4 weeks,
- Patients allergic to ingredients used in the study product,
- Teeth with intrinsic stains caused by other reasons.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2015
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT03237793
Start Date
July 1 2014
End Date
September 1 2015
Last Update
August 8 2017
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