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Clinical Trials/NCT05339178
NCT05339178RecruitingNot Applicable

Evaluation of the Quality of Life of Periodontitis Patients Visiting Supportive Periodontal Therapy - A Prospective Study

Medical University of Vienna1 site in 1 country300 target enrollmentStarted: January 10, 2022Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
300
Locations
1
Primary Endpoint
disease specific OHRQoL (ParoQoL)
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The present prospective study aims to assess the QoL of periodontitis patients during supportive treatment and to relate it to periodontal health (clinical and radiographic data) and treatment stability. Follow-ups after the first cross-sectional assessment are planned after approximately 2.5, 5, 7.5, and 10 years.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 130 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All patients returning for supportive therapy on a regular basis after active periodontal treatment will be asked for participation if they are in supportive therapy for at least 1 year.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

disease specific OHRQoL (ParoQoL)

Time Frame: after 10 years

Secondary Outcomes

  • Oral Health Impact Profile (OHIP)(after 10 years)
  • perceived stress scale (PSS)(after 10 years)
  • overall health status of the patients (EQ5D-5L)(after 10 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kristina Bertl

Principal Investigator

Medical University of Vienna

Study Sites (1)

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