Treatment of Peri-implant Mucositis on Incongruous Dental Prostheses Versus Congruous

Bleeding of Subgingival Space Clinical Trial

Official title:

Impact of Non-surgical Treatment of Peri-implant Mucositis on Incongruous Dental Prostheses Versus Congruous on a Single Tooth Restoration

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05923554
• Other study ID #: 22-150-PO
• Status: Recruiting
• Phase: N/A
• Start date: May 25, 2023
• Est. completion date: October 31, 2023

Study information

• Verified date: June 2023
• Source: University of Catania
• Contact: Gaetano Isola
• Phone: 0953785652
• Email: gaetano.isola[@]unict.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of the present study was to test the hypothesis that non-surgical periodontal therapy on peri-implant mucositis resolution results in a greater clinical improvement in patients with congruous versus non-congruous single dental implant restoration.

Description:

The aim of the present study was to test the hypothesis that non-surgical periodontal therapy on peri-implant mucositis resolution results in a greater clinical improvement in patients with congruous versus non-congruous single dental implant restoration by comparing two groups of patients with peri-implant mucositis.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 56
• Est. completion date: October 31, 2023
• Est. primary completion date: October 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• peri-implant mucositis

• bleeding on probing and/or a gingival index <1 at least at one site at baseline

• absence of peri-implant bone loss during the last 2 years before baseline

Exclusion Criteria:

• Periodontal disease

• Systemic diseases

Related Conditions & MeSH terms

• Bleeding of Subgingival Space
• Mucositis

Intervention

Other:
• Changes in Probing Depth to non-surgical periodontal therapy
Changes in Probing Depth following non surgical periodontal treatment performed with hand and ultrasonic tips

Locations

Country	Name	City	State
Italy	AOU Policlinico G. Rodolico	Catania

Sponsors (1)

Lead Sponsor	Collaborator
University of Catania

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bleeding on probing change % reduction	Reduction in bleeding on probing % change following non surgical periodontal therapy	6-months
Secondary	Reduction of probing depth in mm	Reduction of probing depth following non surgical periodontal therapy	6-months