About this trial
* 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.
Eligibility criteria
Qualifiers
Age between 18-45 years.
Good oral hygiene.
Active primary class I carious lesions on vital molar teeth with ICDAS score 3
Patients complaining of sensitivity to air and osmotic stimulus.
Disqualifiers
Excessive tooth wear due to clenching or abnormal habits.
Traumatic occlusion.
Periodontal or gingival disease.
Patients using analgesics and/or anti-inflammatory medicine.
Trial design
Treatments tested in this trial
- Drug/Agent: Gluma Desensitizer
- Drug/Agent: No desensitizer (Control)
Treatment groups
Sponsors and collaborators
Beenish Hassan
Lead sponsor
Margalla Institute of Health Sciences
Sponsor institution