Influence of Local Doxycycline on the Outcomes of Periodontal Regeneration

Status Active, not recruiting

Clinical Trial Summary

In this double-blinded randomized clinical trial, patients presenting periodontal intrabony defects requiring regenerative surgery and showing BoP will be included. Experimental sites at T-0 will be randomly treated with gentle debridement and administration of local DOX (test group) or with debridement alone (control group). After 2 weeks (T-1), defects will be treated by means of minimally invasive surgical technique. 14 days after the surgery (T-2) the EHI will be evaluated by a blinded examiner. Patients will be recalled each 2 months up to 12 months (T-3). At T-0, T-1 and T-3 periodontal examination and radiographic analysis will be done.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Periodontal Diseases

Clinical Trial Details

NCT number	NCT05878353
Study type	Interventional
Source	University of Turin, Italy
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 1, 2023
Completion date	February 15, 2024

View Details

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