Analysis of bacterial formation, composition and growth on implant temporary crow

Not Applicable

Not yet recruiting

• Conditions: Peri-implant infection/diseases; Dental implant infection; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12622000707763
• Lead Sponsor: The University of Sydney

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-05-17
• Last Update Posted: 6 June 2022

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

The inclusion criteria for the potential participants include:
•Adults aged 21 years and more that are suitable for dental implants treatment or have received already an implant that needs to be restored in the posterior region (non-esthetic sites).
•Medically healthy without any active dental or periodontal diseases.
•Good oral hygiene assessed by a full-mouth bleeding and plaque score.
•Participants need to be willing to provide informed consent and willing to participate and comply with the study requirements.

Exclusion Criteria

•Participants that are not eligible for dental implant treatment. Absolute contraindications to dental implant treatment include recent myocardial infarction and cerebrovascular accident, valvular prosthesis surgery, immunosuppression, bleeding issues, active treatment of malignancy, drug abuse, psychiatric illness, and intravenous bisphosphonate use (Hwang & Wang, 2006).
•Participants with failing/compromised implants or peri-implantitis.
•Implant sites located in aesthetic zones, and sites that require tissue augmentation / grafting.
•Pregnant/lactating patients
•Antibiotic therapy in the last 3 months.
•Completely edentulous patients

Study & Design

• Study Type: Observational
• Study Design: Not specified