U.S., April 21 -- ClinicalTrials.gov registry received information related to the study (NCT07540299) titled 'Dipotassium Oxalate for Postoperative Sensitivity in NCCLs' on April 13.
Brief Summary: Postoperative sensitivity is a common complication following Class V composite restorations, particularly in non-carious cervical lesions (NCCLs). This randomized controlled trial aims to evaluate the effectiveness of dipotassium oxalate as a pre-treatment agent in reducing postoperative sensitivity.
A total of 64 participants will be randomly assigned into two groups: an intervention group receiving dipotassium oxalate prior to adhesive application, and a control group receiving standard adhesive protocol without pretreatment. Sensitivity will...