drugset / Trial / NCT04036890

Local Minocycline in Patients Under Supportive Periodontal Therapy

NCT04036890

Phase 4 Completed 68 enrolled National Dental Centre, Singapore
RandomizedParallel-groupTriple-blindTreatment

Summary

The aims of the present study are to assess the significance of the adjunctive effect of the subgingival application of a 2% minocycline hydrochloride controlled-delivery system (MHS) in comparison to subgingival instrumentation with application of a placebo gel, 3 months after therapy in subjects with recurrent periodontitis undergoing supportive periodontal therapy (SPT) and to assess the substantivity of the gel attributable to the adjunctive delivery of the medication that is detected at 3 months during a 9-month period of regular SPT. Recurrent periodontitis will be defined as sites with residual periodontal probing depths and bleeding on probing after completion of initial periodontal therapy. This will include both persistent and recurrent periodontitis, where persistent means the residual periodontal site after initial periodontal therapy, and recurrent means the site which was improved by initial periodontal therapy, but disease recurred.

Timeline

Start
2016-06-03
Primary completion
2019-10-18
Completion
2019-10-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Minocycline Small molecule 10 mg Other

Indications