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Study to compare the effect of laser and desensitising gel in treatment of increased sensitivity of teeth .

Not Applicable
Conditions
Health Condition 1: null- Patients having hypersensitive teeth in mild to moderate periodontitis cases
Registration Number
CTRI/2013/11/004176
Lead Sponsor
Shreya Palyekar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

1)Patient with age group 18- 55 yrs.

2) Both males & females.

3) Subject should have at least 3 hypersensitive teeth & one non sensitive but dentin exposed tooth, following air blast evaporative stimulus at the screening & baseline visit.

4) All teeth except molar are included in trial.

5)Patient is willing for treatment & ready to give written consent.

6) Hypersensitivity post scaling and root planing in patient with mild to moderate periodontitis with recession

Exclusion Criteria

1. Current desensitizing therapy.

2. Medical (including psychiatric) and pharmacotherapeutic histories that may compromise the protocol â?? including the chronic use of anti-inflammatory, analgesic and mind-altering drugs.

3. Pregnancy or breast feeding.

4. Allergies and idiosyncratic responses to product ingredients.

5. Eating disorders (detailed written dietary history and investigation into bulimia and other dietary problem).

6. Systemic conditions that are etiologic or predisposing to dentine hypersensitivity (e.g., chronic acid regurgitation).

7. Excessive dietary or environmental exposure to acids.

8. Orthodontic appliance treatment within previous 3 months.

10. Teeth or supporting structures with any other painful pathology or defects.

11. Teeth restored in the preceding 3months.

12. Abutment teeth for fixed or removable prostheses.

13. Crowned teeth.

14. Extensively restored teeth and those with restorations extending into the test area.

15. Erratic & inconsistent responder will be identified and eliminated from trial

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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