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NCT05339178 Clinical Trial

Quality of Life of Periodontitis Patients Visiting Supportive Periodontal Therapy

Quality of Life Clinical Trial

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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05339178
Other study ID # 1398/2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 10, 2022
Est. completion date December 2033

Study information
Verified date April 2022
Source Medical University of Vienna
Contact Kristina Bertl
Phone 00436645151194
Email kristina.bertl@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 300
Est. completion date December 2033
Est. primary completion date December 2032
Accepts healthy volunteers No
Gender All
Age group 18 Years to 130 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Austria Division of Oral Surgery, School of Dentistry, Medical University of Vienna Vienna

Sponsors (1)
Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome
Type Measure Description Time frame Safety issue
Primary disease specific OHRQoL (ParoQoL) at baseline
Primary disease specific OHRQoL (ParoQoL) after 2.5 years
Primary disease specific OHRQoL (ParoQoL) after 5 years
Primary disease specific OHRQoL (ParoQoL) after 7.5 years
Primary disease specific OHRQoL (ParoQoL) after 10 years
Secondary Oral Health Impact Profile (OHIP) at baseline
Secondary perceived stress scale (PSS) at baseline
Secondary overall health status of the patients (EQ5D-5L) at baseline
Secondary Oral Health Impact Profile (OHIP) after 2.5 years
Secondary perceived stress scale (PSS) after 2.5 years
Secondary overall health status of the patients (EQ5D-5L) after 2.5 years
Secondary Oral Health Impact Profile (OHIP) after 5 years
Secondary perceived stress scale (PSS) after 5 years
Secondary overall health status of the patients (EQ5D-5L) after 5 years
Secondary Oral Health Impact Profile (OHIP) after 7.5 years
Secondary perceived stress scale (PSS) after 7.5 years
Secondary overall health status of the patients (EQ5D-5L) after 7.5 years
Secondary Oral Health Impact Profile (OHIP) after 10 years
Secondary perceived stress scale (PSS) after 10 years
Secondary overall health status of the patients (EQ5D-5L) after 10 years
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