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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04299347
Other study ID # PR001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 29, 2018
Est. completion date March 3, 2020

Study information

Verified date March 2020
Source University of Siena
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the present study is to understand the influence that marginal/subgingival restorations exert on the surrounding periodontal tissues. Even though proximal restorations are routine in everyday clinical practice, few information is available as to whether or not they may have a detrimental effect on the supracrestal tissue attachment.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 3, 2020
Est. primary completion date June 29, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- an age range 18-70 years

- a good general health

- the ability to understand the phases of the trial and to stick to them for the whole length of the study

- the ability of will to release a written informed consent

- presence of a marginal cavity or a 2mm subgingival cavity

- presence of a cavity subgingival > 2mm

Exclusion Criteria:

- PPD>4mm

- patients affected by active periodontal disease

- patients smoking more than 10 cigarettes/pipes per day

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy AOUS Siena

Sponsors (1)

Lead Sponsor Collaborator
University of Siena

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bleeding on Probing bleeding from the gingival sulcus when probing 12 months
Secondary radiographic distance from the caries/margin of the restoration to the bone crest LInear measurement between the most apical level of the restoration to the bone crest 12 months
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