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Comparison of the Effectiveness of Combined Diode Laser and GLUMA Bonding Therapy with Combined Diode Laser and 5% Sodium Fluoride Varnish in Patients with Increased Dentin Sensitivity

Comparison of the Effectiveness of Combined Diode Laser and GLUMA Bonding Therapy with Combined Diode Laser and 5% Sodium Fluoride Varnish in Patients with Increased Dentin Sensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201219049759N1
Enrollment
45
Registered
2021-01-28
Start date
2018-10-23
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Condition 1: Increased dentin sensitivity. Condition 2: diode laser. Condition 3: GLUMA bonding. Condition 4: 5% Sodium Fluoride Varnish.

Interventions

Intervention 1: Intervention group 1 (bonding): For this purpose, we use the solution of Kulzer GmbH, Germany GLUMA Desensitizer, which in a 5 ml bottle contains 5% glutaraldehyde, 35% HEMA-G and dist

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: good general health Having at least 3 teeth with hypersensitivity to contact stimulus or air blast Agree to follow up for 1 month

Exclusion criteria

Exclusion criteria: Having benign or malignant oral disease long-term use of the drug having caries in the affected or adjacent tooth enamel cracking congenital defects in the enamel or dentin tooth restoration orthodontic procedures periodontal disease history of vital bleaching history of Periodontal surgery or treatment of hypersensitivity during the last 6 months history of non-surgical treatment of periodontal disease during the past 3 months use of mouthwash containing allergens pregnancy or lactation use of antidepressants and analgesics history of allergies to components Various treatment therapies bruxism abrasion

Design outcomes

Primary

MeasureTime frame
Pain intensity on the VAS scale. Timepoint: Before the intervention, immediately after the intervention and at intervals of 2, 7 days and 1 month after the intervention. Method of measurement: VAS scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Anbari

Shahid Beheshti University of Medical Sciences

fahimeh.anbari@gmail.com098 21 22175351

Outcome results

None listed

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