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Clinical Trial Summary

the aim of our study is to enhance the dissolution and subsequently the local penetration of the drug through the sulcus in addition to controlling the drug release so that, the drug could be potentially absorbed.


Clinical Trial Description

Patients will be divided randomly into three groups: Group (I);will be treated with subgingival debridement and subgengival injection of chitosan 2% gel containing a microsponges formulated (SV), Group (II); will be treated with subgingival debridement and subgingival injection of chitosan 2% gel containing free (SV) and Group (III); will be treated by subgingival debridement and placebo gel injected subgingivally. Pocket depth and clinical attachment loss bone gain were recorded preoperative and six months postoperative for all groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04836078
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase Early Phase 1
Start date February 10, 2020
Completion date October 10, 2020

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