Clinical Trials Directory

Trials / Completed

CompletedNCT04983849

Evaluation of Metronidazole Hydrogel 25% in Stage II and III Periodontitis

Evaluation of Effects of Subgingival Administration of Metronidazole Hydrogel 25% in Stage II and III Periodontitis: Randomized, Split Mouth, Single-blind Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of L'Aquila · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

A randomized clinical trial will be performed single-blind to evaluate the effectiveness of sublingual metronidazole hydrogel 25 % in periodontitis.

Detailed description

A randomized clinical trial will be performed single-blind to evaluate the effectiveness of sublingual metronidazole hydrogel 25 % in periodontitis in stage II and III. At least 40 volunteers between the age of 18 and 80, will be enlisted, with the need to perform the SRP. In half of the mouth will be used the metronidazole hydrogel 25%, while in the other half no drugs will be used of delivered. The study will be carried out in accordance with the Helsinki Declaration and the Protocol will be submitted to the Internal Review Board of the University to obtain authorization. Afterwards, the protocol will be recorded on the databa-se clinicaltrials.gov for clinical trials. The protocol respects the SPIRIT parameters for the compilation of protocols on clinical trials and the study will respect the parameters of CONSORT sta-tement on randomized clinical trials.

Conditions

Interventions

TypeNameDescription
DRUGmetronidazole hydrogelscaling and root planning in adjunct to the use of metronidazole in the periodontal pocket
PROCEDUREscaling and root planningscaling and root planning

Timeline

Start date
2021-07-07
Primary completion
2021-07-07
Completion
2021-07-07
First posted
2021-07-30
Last updated
2023-12-12

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04983849. Inclusion in this directory is not an endorsement.