Clinical Trial

Gluma Compared With Bonding Agent for Post-operative Sensitivity Following Composite Restorations

Not Yet Recruiting Phase 2/3
View on ClinicalTrials.gov →
Record status
This record was last updated September 23, 2025 (before its estimated May 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
* The aim of this study is to compare the effectiveness of Gluma desensitizer in reducing post-operative sensitivity following composite restorations in posterior teeth. -Patients visiting OPD will be selected after fulfilment of inclusion criteria. Patients aged 18-45 meeting inclusion criteria and presenting with active primary class I carious lesions on vital molar teeth with ICDAS score 3 will be randomly assigned into two groups: -Group A: Patients will be provided with Gluma desensitizer, Universal Bonding agent and Composite restoration and -Group B: Patients will receive Universal bonding agent and Composite restoration. -The progress of treatment will be followed up immediately (baseline) and at regular follow up visits at 1 week, 1 month and 3 months. * Post-operative sensitivity will be assessed using an air stimulus and rated on a numeric rating scale for post-operative sensitivity assessment ranging from 0 to 10.
Trial Details
NCT Number NCT07188142
Lead Sponsor Beenish Hassan
Conditions Post-operative Sensitivity, Dentin Hypersensitivity, Dental Caries, Tooth Sensitivity After Composite Restorations, Post-operative Sensitivity After Class I Composite Restorations
Enrollment 60 participants
Start Date 2025-12-01
Primary Completion 2026-05-01 (estimated)
Study Completion 2026-06-01 (estimated)
Updated on ClinicalTrials.gov 2025-09-23