Impact of Laser-modified Abutment Topography on Peri-implant Mucosal Integration

NCT ID: NCT03982615

Last Updated: 2021-03-26

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-05-08
• Study Completion Date: 2021-12-31

Brief Summary

This study is a prospective randomized split mouth study intended to evaluate the healing and health of peri-implant mucosal tissue following placement of titanium abutments with or without laser-etching.

Each subject will receive two implants. Following placement of the two 4.2mm diameter implants, one implant will receive (by randomization) a laser-etched abutment ('Laser-Lok'). The other implant will receive a standard, non-etched healing abutment. Subjects will be sequentially subdivided into four groups (n=5) and scheduled for a biopsy of the peri-implant tissues of both implants at either 8 weeks, 4 weeks, 2 weeks or 1 week after implant surgery. These biopsies, about the size of a grain of rice, will be analyzed using immunohistochemical and RNASeq techniques to identify molecular changes in response to laser etching.

At approximately 8 weeks after implant surgery, subjects will have abutments removed from both implants and digital impressions taken for final crown fabrication. At approximately 11-12 weeks after implant surgery, final crowns will be placed. Subjects return to clinic at approximately 1 year post surgery for a final study visit to assess the peri-implant mucosa surrounding both implants as measured by bleeding upon probing, probing depth and peri-apical radiography.

Detailed Description

A dental implant is an artificial "root" for a missing tooth made out of surgical grade metals, usually titanium, which is placed in the jaw. An implant is designed to provide a strong foundation for an artificial replacement tooth, also called a "crown". An abutment is a medical grade connector, usually made of titanium, which is placed on top of the implant, and is designed to hold and connect the crown to the implant. A crown, also called a "dental cap" is an artificial tooth, generally made of porcelain or surgical grade metals.

Osseointegration is defined as the fusion of a dental implant and abutment with the surrounding jaw bone and is a critical step during implant therapy. During this process, the titanium and bone need to become one solid structure (without any intervening inflammatory mucosal tissue in between) for optimum strength and viability.

It is hypothesized that use of an abutment whose surface has been etched with a laser ("laser-etched") will enhance the attachment of the abutment to the surrounding bone and mucosal tissue and optimize healing.

The goal of this research is to compare, by split mouth design, the healing process of peri-implant mucosal tissue adjacent to a standard healing abutment (not laser-etched) versus mucosal tissue healing adjacent to a laser-etched abutment .

Each subject will receive two implants. One implant will receive (by randomization) a standard titanium healing abutment that is not laser-etched. The other implant will receive a laser-etched ("Laser-Lok") abutment. Subjects will be sequentially subdivided into 4 groups (n=5) and scheduled for a biopsy of peri-implant tissue at both implant sites at either 8 weeks, 4 weeks, 2 weeks or 1 week after implant surgery. The biopsies, about the size of a grain of rice, will be analyzed using histological and molecular techniques to identify cellular changes in response to laser-etching.

Approximately 8 weeks after implant placement, subject will have abutments removed and digital impressions taken for final crown fabrication. At approximately 11-12 weeks post implant placement, final crowns will be placed. Subjects return to clinic at approximately 1 year post surgery for a final study visit to assess the peri-implant mucosa around both implants as measured by bleeding upon probing, probing depth and peri-apical radiography.

Conditions

Dental Implant Failure Nos

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Laser-Lok abutment

Laser-etched abutment

Group Type: EXPERIMENTAL

Laser-Lok abutment

Intervention Type: DEVICE

Each subject will receive two dental implants. One implant will receive (by randomization) a laser-etched ("Laser-Lok") abutment.

Standard Healing abutment

Standard abutment which is not laser-etched

Group Type: ACTIVE_COMPARATOR

Standard healing abutment

Intervention Type: DEVICE

Each subject will receive two dental implants. One implant will receive (by randomization) receive a standard healing abutment (not laser-etched).

Interventions

Laser-Lok abutment

Each subject will receive two dental implants. One implant will receive (by randomization) a laser-etched ("Laser-Lok") abutment.

Intervention Type: DEVICE

Standard healing abutment

Each subject will receive two dental implants. One implant will receive (by randomization) receive a standard healing abutment (not laser-etched).

Intervention Type: DEVICE

Other Intervention Names

laser-etched abutment; non-laser etched abutment

Eligibility Criteria

Inclusion Criteria

• Adult, able to provide informed written consent and available for 1 year follow-up visit
• Have 2 edentulous sites requiring single tooth implants for restoration in two separate quadrants
• Implant sites must be restorable with 4.2mm diameter implants
• Have natural teeth adjacent (at least unilaterally) to proposed implant sites
• Able to pay for implant crowns at UIC College of Dentistry postgraduate fees to complete treatment

Exclusion Criteria

• Uncontrolled/rampant caries or periodontal disease
• Unable to demonstrate adequate home oral hygiene
• smoker within the past 6 months
• ASA Class 3+, immune-compromised
• Pregnant or planning to become pregnant within 6 months
• Severe bruxism
• History of bisphosphonate use
• Bone grafting required for implant placement
• Missing tooth is too small to be restored using a 4.2mm implant

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

BioHorizons, Inc.

INDUSTRY

Sponsor Role: collaborator

University of Illinois at Chicago

OTHER

Sponsor Role: lead

Responsible Party

Lyndon F Cooper

Associate Dean of Research, Chair-Department of Oral Biology, College of Dentistry

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Lyndon F Cooper, DDS, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Illinois at Chicago College of Dentistry

Locations

University of Illinois at Chicago, College of Dentistry, Clinical Research Center

Chicago, Illinois, United States

Countries

United States

References

Leong A, De Kok I, Mendonca D, Cooper LF. Molecular Assessment of Human Peri-implant Mucosal Healing at Laser-Modified and Machined Titanium Abutments. Int J Oral Maxillofac Implants. 2018 Jul/Aug;33(4):895-904. doi: 10.11607/jomi.6367.

Reference Type: BACKGROUND

PMID: 30025007 (View on PubMed)

Other Identifiers

2018-1358

Identifier Type: -

Identifier Source: org_study_id