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NCT06028867

Validation of the Clinical and Antimicrobial Effectiveness of a Clorexidine and Sodium DNA Based Mouthwash in Patients With Stage III and IV Periodontitis

Completed NA Last updated 8 May 2024
What this trial tests

NA trial testing Non-surgical periodontal treatment in Periodontitis in 56 participants. Completed in 20 April 2024.

Timeline
24 January 2020
Primary endpoint
30 January 2024
20 April 2024

Quick facts

Lead sponsorUniversity of Catania
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment56
Start date24 January 2020
Primary completion30 January 2024
Estimated completion20 April 2024
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

University of Catania

Who can join

Adults 18 to 75, any sex, with Periodontitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Sodium DNA has several properties that may be beneficial in the management of bacterial biofilm in periodontitis. The aim of this RCT study is to clinically evaluate the antimicrobial and oral biofilm control properties of two mouthwashes containing Chlorhexidine 0.12% + Sodium DNA and Chlorhexidine 0.20% at two weeks, compared with a placebo, on patients with stage III or IV periodontitis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Non-surgical periodontal treatment

Trials testing the same drug.

Other recruiting trials for Periodontitis

Currently open trials in the same condition.

Other University of Catania trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06028867.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing