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Clinical Trials/TCTR20240501003
TCTR20240501003
Completed
Not Applicable

Inflammatory responses of peri-implant crevicular fluid on different dental implant abutment materials after 6-months functional loading: A randomized clinical controlled trial

Faculty of Dentistry, Chulalongkorn University0 sites16 target enrollmentMay 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Age 18 - 60 years old.Healthy or with well-controlled systemic diseases.Patients who have been treated with single tooth implant in esthetic zone either with or without bone graft on anterior teeth including upper or lower canines, lateral incisors and central incisors at crestal bone level.Screw retained or screw-cement retained implants.Sufficient keratinized gingiva of width of at least 4 mm.Undergone oral prophylaxis treatment and instructions after implant placement.
Sponsor
Faculty of Dentistry, Chulalongkorn University
Enrollment
16
Status
Completed
Last Updated
last year

Overview

Brief Summary

Within the limitations of the present study, titanium base abutments presented no significant differences in terms of inflammatory responses compared to titanium abutments after 6 months functional loading. Thus, when used to support single crowns, titanium base can be a feasible treatment alternative to titanium abutments.

Registry
who.int
Start Date
May 1, 2024
End Date
December 15, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Faculty of Dentistry, Chulalongkorn University

Eligibility Criteria

Inclusion Criteria

  • 1\. healthy or with well\-controlled systemic diseases, 2\. patients who have been treated with single tooth implant in esthetic zone (Neodent\-Straumann or Straumann, Switzerland) either with or without bone graft on anterior teeth including upper or lower canines, lateral incisors and central incisors at crestal bone level, 3\. screw retained or screw\-cement retained implants, 4\. sufficient keratinized gingiva of width of at least 4 mm, and 5\. undergone oral prophylaxis treatment and instructions after implant placement.

Exclusion Criteria

  • 1\. medical or general contraindication to the surgical procedure (American Society of Anesthesiologists (ASA) status III), 2\. smokers (at least 10 cigarettes per day), 3\. poor plaque control or having untreated active periodontal disease, 4\. having acute infection including severe swelling of the gingiva, suppuration, and abscess, and 5\. being pregnant.

Outcomes

Primary Outcomes

Not specified

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