[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dentin-hypersensitivity-post-operative-sensitivity-control\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dentin-hypersensitivity-post-operative-sensitivity-control":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100634485","dipotassium-oxalate-for-postoperative-sensitivity-in-nccls-100634485",false,"NCT07540299","Dipotassium Oxalate for Postoperative Sensitivity in NCCLs","Comparative Evaluation of Dipotassium Oxalate in Postoperative Sensitivity Control in Class V Composite Restorations: A Randomized Controlled Trial","DIPOX-RCT","Inclusion Criteria:\n\n* Individuals aged 30 to 45 years.\n* Presence of at least one tooth with a non-carious cervical lesion (Class V) with a lesion depth of ≥1 mm, requiring restorative treatment.\n* The NCCL must show some symptoms\u002Fsigns of pre-op sensitivity on applying stimulus (i.e Air burst \u002F ethyl chloride spray) and will be recorded.\n* The involved teeth must be vital and show no signs or symptoms of irreversible pulpitis or necrosis.\n* Subjects must be willing to provide written informed consent and commit to the study's follow-up schedule.\n* Subjects with fair to good oral hygiene as determined by a simplified oral hygiene index (OHI-S score ≤2).\n\nExclusion Criteria:\n\n* Presence of carious lesions or restored teeth with existing secondary caries\n* Any tooth with pulpal involvement, previous root canal therapy, or periapical pathology.\n* Teeth with chronic periodontal disease( BPE score 3 and above.).\n* Individuals regularly using Desensitizing toothpastes, NSAIDs, antidepressants, or any other pain-modulating drugs that may alter sensitivity reporting.","ALL","30 Years","45 Years",{"count":21,"type":22},64,"ESTIMATED","INTERVENTIONAL",[25],"NA","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.\n\nA 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 be assessed using a Visual Analog Scale (VAS) in response to cold and air stimuli at baseline, 24 hours, 7 days, and 30 days.\n\nThe study aims to determine whether dipotassium oxalate significantly reduces postoperative sensitivity and can be incorporated into routine restorative dental practice.",[28],"Dentin Hypersensitivity, Post Operative Sensitivity Control",[30,31,32,33,34],"Dipotassium Oxalate","Postoperative Sensitivity","Composite Restoration","NCCL","Dentin Hypersensitivity","NOT_YET_RECRUITING","2026-04-18",{"date":38,"type":39},"2026-04-22","ACTUAL",{"date":41,"type":22},"2026-06-01",{"date":43,"type":22},"2026-10-01",{"name":45,"class":46},"Postgraduate Medical Institute, Lahore","OTHER"]