Skip to content

Comparative evaluation of sodium flouride varnish laser and their combination to treat dental hypersensitivity.

Comparative Evaluation Of Sodium Fluoride Varnish , Diode Laser and Their Combination To Reduce Dental Hypersensitivity: A Randomized Clinical Study. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068926
Enrollment
36
Registered
2024-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K039- Disease of hard tissues of teeth,unspecified

Interventions

Intervention1: diode laser and combination of diode laser and flouride varnish: 980 nm diode laser (DL) irradiation alone and 980 nm diode laser irradiation plus flourodip bioactive varnish combinatio

Sponsors

DrDevashree Darak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Systemically healthy both male and female patients between 18-70 years of age will be included in the study. 2. Patients with good oral hygiene, and clinically demonstrable dentinal hypersensitivitywill be included in the study. 3. Participants who have more than two sensitive teeth with a Schiff sensitivity score of = 2 will be included in the study. 4. Patients with pre-operative VAS scoresof more than 3 on application of air/ cold will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to sodium fluoride or known allergy to any toothpaste containing fluoride will be excluded from the study. 2. Patients with any systemic or psychological diseases, constant use of analgesics, anti-inflammatory drugs, or allergic responses to dental products will be excluded from the study. 3. Teeth with carious lesions, defective restorations, fractures, prosthesis or orthodontics appliances, periodontal pockets, mobility, or evidence of pulpits will be excluded from the study. 4. In addition, those who have used any desensitizing agents or undergone any periodontal surgery in the last 6 months were excluded from the study 5. Patientstaking any analgesics, antibiotics, sedatives, and anti-anxiety drugs on regular basis or before 24 hours of treatment will be excluded. 6. Pregnant and lactating patients will be excluded from study.

Design outcomes

Primary

MeasureTime frame
Reduction in post-opeative sensitivity after use of flouride varnish and diode laser .Timepoint: 24 hours and 1 week

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr. Deebah Choudhary

K M shah dental college and hospital

deebahchoudhary@yahoo.in9018872050

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026