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Recruiting NCT05339178

Quality of Life of Periodontitis Patients Visiting Supportive Periodontal Therapy

Observational Quality of Life Periodontal Diseases

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Quality of Life, Periodontal Diseases. Basic parameters: 18 years — 130 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Austria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Primary outcome measures

  • disease specific OHRQoL (ParoQoL) [Time frame: at baseline]
  • disease specific OHRQoL (ParoQoL) [Time frame: after 2.5 years]
  • disease specific OHRQoL (ParoQoL) [Time frame: after 5 years]
  • disease specific OHRQoL (ParoQoL) [Time frame: after 7.5 years]
  • disease specific OHRQoL (ParoQoL) [Time frame: after 10 years]
Secondary outcome measures (12)
  • Oral Health Impact Profile (OHIP) [Time frame: at baseline]
  • perceived stress scale (PSS) [Time frame: at baseline]
  • overall health status of the patients (EQ5D-5L) [Time frame: at baseline]
  • Oral Health Impact Profile (OHIP) [Time frame: after 2.5 years]
  • perceived stress scale (PSS) [Time frame: after 2.5 years]
  • overall health status of the patients (EQ5D-5L) [Time frame: after 2.5 years]
  • Oral Health Impact Profile (OHIP) [Time frame: after 5 years]
  • perceived stress scale (PSS) [Time frame: after 5 years]
  • overall health status of the patients (EQ5D-5L) [Time frame: after 5 years]
  • Oral Health Impact Profile (OHIP) [Time frame: after 7.5 years]
  • perceived stress scale (PSS) [Time frame: after 7.5 years]
  • overall health status of the patients (EQ5D-5L) [Time frame: after 7.5 years]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Austria · 1 center
  • Division of Oral Surgery, School of Dentistry, Medical University of Vienna — Vienna

Identifiers

NCT: NCT05339178 · 1398/2021

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗