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NCT05332327 Clinical Trial

Comparison of the Accuracy of Different Periodontal Probes for Peri-implant Pocket Registration

Peri-Implantitis Clinical Trial

Official title:
Comparison of the Accuracy of Different Periodontal Probes for Peri-implant Pocket Registration

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05332327
Other study ID # 2020-01019/2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 8, 2020
Est. completion date February 13, 2023

Study information
Verified date March 2023
Source Malmö University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Various types of periodontal probes (e.g., metal probes, plastic/bendable probes, electronic periodontal probes) are used for peri-implant pocket depth registration; however, depending on the shape and size of the prosthetic restoration an accurate peri-implant pocket registration might be impeded with standard metal probes. There is currently no systematic assessment of which probe is more accurate in peri-implant pocket registration. Therefore, peri-implant pocket registration of 50 patients with a screw-retained prosthetic restoration will be recorded with 3 different periodontal probes; i.e., with a metal probe, with a plastic probe, and with an automatic periodontal probe, before and after removal of the prosthetic restoration.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date February 13, 2023
Est. primary completion date February 13, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - screw-retained prosthetic implant restoration Exclusion Criteria: - cemented prosthetic implant restoration

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden Department of Periodontology, Malmö University Malmö

Sponsors (1)
Lead Sponsor Collaborator
Malmö University

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary peri-implant probing pocket depth peri-implant probing pocket depth in mm 1 day (single measurement)
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