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NCT06113874 Clinical Trial

The Influence of Desensitizing Agent on Postoperative Sensitivity in Posterior Composite Restoration

Dentin Hypersensitivity Clinical Trial

Official title:
The Influence of Desensitizing Agent on Postoperative Sensitivity in Posterior Composite Restoration: A Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06113874
Other study ID # 7/22
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 5, 2022
Est. completion date August 30, 2023

Study information
Verified date October 2023
Source University of Alexandria
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to investigate the influence of desensitizing agents on reducing post-operative sensitivity in posterior composite.

Recruitment information / eligibility
Status Completed
Enrollment 10
Est. completion date August 30, 2023
Est. primary completion date August 5, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Patients having active primary class I carious lesions on vital molar teeth either in the middle or the inner third of dentin in the three quadrants of each patients. - Teeth having a positive reaction to vitality test (cold test), no signs of pulp inflammation, or spontaneous pain before treatment. - Preoperative radiographic record of the carious lesions. - Buccolingual width is no more than half the inter-cuspal distance Exclusion Criteria: - Excessive tooth wear due to clenching or abnormal habits. - Patients with direct occlusal contact by antagonist cusp (traumatic occlusion). - Patients with periodontal or gingival disease. - Patients using analgesics and/or anti-inflammatory medicine.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Hurriseal desensitizer
Patients will receive Hurriseal desensitizing agent and universal bond and composite. Cavities will be restored with light-cured composite resin following the application of bonding agent.
• Gluma desensitizer
Patients will receive Gluma desensitizing agent and universal bond and composite. Cavities will be restored with light-cured composite resin following the application of bonding agent.

Locations
Country Name City State
Egypt Faculty of Dentistry, Alexandria University Alexandria

Sponsors (1)
Lead Sponsor Collaborator
Nourhan M.Aly

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hypersensitivity assessment Air spray will be applied from a 2-mm distance on to the occlusal for 3 seconds. The severity of patients' pain/sensitivity will be recorded using (0-10) numerical rating scale. The score will be ranged from 0 (No pain) to 10 (maximum pain) up to 12 months
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