Severity of Periodontal Recession and Associated Risk Factors in France.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

240 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-01-10

Study Completion Date

2021-02-05

Brief Summary

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The severity of periodontal recessions for each examined patient during dental consultation was evaluated. Moreover, the description of the number of periodontal recessions in patients with good health during dental consultation, the associated risk factors and evaluation of the number of recessions which need surgical therapy were realized.

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Detailed Description

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Conditions

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Periodontal Recessions

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Case -

Patient presenting one or more periodontal recession more than 1mm of height

Clinical examination of gingival tissues

Intervention Type OTHER

Measure of the periodontal recession

Control-

Patient presenting no periodontal recession or recession of less than 1 mm of height

Clinical examination of gingival tissues

Intervention Type OTHER

Measure of the periodontal recession

Interventions

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Clinical examination of gingival tissues

Measure of the periodontal recession

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Case:

* patients aged from 20 to 50 years
* patients with recession of more than 1mm
* patient with good health
* patients who aggreed to participate to the study

Controls:

* patients aged from 20 to 50 years
* patients with no recession or recession less than 1mm
* patient with good health
* patients who aggreed to participate to the study

Exclusion Criteria

* patients with periodontitis
* patients with recession of Class III and IV of modified Miller classification
* patients with previous muco-gingival surgery
* patients pregnant, breatheeding
* patients refusing to participate to the study

Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes