Soft Tissue Responses Around Nanostructured Calcium-phosphate-coated Implant Abutments on Dental Implants: Histological, Genetic and Clinical Evaluation in Smokers and Non-smokers. (STRANDI)

• Baseline:

  • Standard preparation of the osteotomy
  • Placement of 2 dental implants
  • On each implant one of both types of healing abutments is placed
  • Suturing
  • Standardized radiography to measure bone-levels at baseline
  • Digital impression of the surrounding gingiva with an intra-oral scanner (a non-invasive method) to measure the baseline level of the gingiva

• 2 weeks after Baseline:

  o Removal of the sutures

• 4 weeks after Baseline:

  • A 2nd digital impression of the soft tissue with an intra-oral scanner
  • Collecting crevicular fluid by placing paperpoints in the provided apertures in the healing abutments for 60 seconds without bleeding.
  • Measuring of the pocket depth in the provided apertures in the healing abutments with an automated probe.
  • Removal of the Healing Abutment with the attached soft tissue en-bloque.
  • Placement of a new, regular, Encode Healing Abutment.

• 10 weeks after Baseline:

  • Start of standard prosthetic procedure. In this study we expect that the soft tissue attachment (i.e. the gingival attachment) will be stronger and earlier achieved at the nano-structured healing abutments than at the normal, uncoated healing abutments. This would lead to a more stable soft tissue complex on the long rung and thus providing a more predictable aesthetic outcome. Secondly, a stronger attachment would mean a stronger barrier against micro-organisms and might influence the occurrence of peri-implantitis.

Study Overview

• Status: Completed
• Conditions: Missing Several Teeth; Minimum of 2 Dental Implants Needed
• Intervention / Treatment: Procedure: normal healing abutment; Procedure: nano-structured healing abutment

• Study Type: Interventional
• Enrollment (Actual): 100
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Belgium
  • Ghent, Belgium, 9000
    • Ghent University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patients are eligible for this study if they are in need of minimum 2 dental implants and have sufficient bone to place these implants

Exclusion Criteria:

• All patients with limited bone
• Periodontally compromised patients
• Patients who took antibiotics 3 months before implantation
• Patients with uncontrolled diabetes
• Pregnant patients
• Patients who received radiotherapy in the head/neck region
• Patients under chemotherapy
• Patients who had intravenous use of bisphosphonates

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 2 types of healing abutment; Patients who are in need of minimal 2 dental implants, who will receive both types of healing abutments.	Procedure: normal healing abutment; Patient receives the normal, uncoated healing abutment on 1 of his (minimal 2) dental implants.; Procedure: nano-structured healing abutment; Patient receives the nano-structured healing abutment on 1 of his (minimal 2) dental implants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The soft-tissue attachment around 2 different surfaces at 4 weeks post-implantation.	Genetic evaluation (through Polymerase Chain Reaction, PCR, the tissue will be detected for certain growth factors), histomorphometric analysis to measure the actual percentage of the surface on which the gingiva is attached to, clinical evaluation of the strength of the attachment through means of an automated probe.	at 4 weeks post-implantation

Collaborators and Investigators

• Sponsor: University Ghent
• Investigators: Principal Investigator: Hugo De Bruyn, DDS, MSc, PhD, University Ghent

Study record dates

Study Major Dates

• Study Start (Actual): August 1, 2012
• Primary Completion (Actual): January 1, 2015
• Study Completion (Actual): August 1, 2015

Study Registration Dates

• First Submitted: June 13, 2012
• First Submitted That Met QC Criteria: June 13, 2012
• First Posted (Estimate): June 15, 2012

Study Record Updates

• Last Update Posted (Actual): December 1, 2021
• Last Update Submitted That Met QC Criteria: November 18, 2021
• Last Verified: November 1, 2021

More Information

Terms related to this study

• Other Study ID Numbers: 2012/341