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Clinical Trials/NCT04340726
NCT04340726
Completed
Not Applicable

Periimplant Bone Changes in Different Abutment Heights and Insertion Timing in Posterior Mandibular Areas: Results From a Randomized Prospective Clinical Trial

Universidade Católica Portuguesa1 site in 1 countryJanuary 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Implant Failed
Sponsor
Universidade Católica Portuguesa
Locations
1
Primary Endpoint
Marginal bone changes
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study was to compare the influence of the abutment height and insertion timing on early marginal bone loss (MBL) in posterior mandibular partial implant-supported restorations.

Material and methods: The study was planned as a prospective, randomized, controlled parallel group including subjects in need of two implants for the restoration of an edentulous posterior mandibular area. Data were gathered on age, gender, attached gingiva height, bleeding on probing (BoP), smoking habits and previous periodontitis. The patients were allocated into three groups: Group A implants were immediately connected to 2 mm height abutments; Group B implants were immediately connected to 1 mm height abutments; Group C implants were left to heal in a sub-mucosal position and 2 mm abutments were inserted in a second stage surgery. Peri-apical radiographs were taken at the implant surgery (baseline), 4 weeks after surgery (T1), 16 weeks after implant placement at the final restoration delivery (T2) and 1-year after implant placement (T3).

Registry
clinicaltrials.gov
Start Date
January 1, 2015
End Date
December 31, 2015
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tiago Borges

Professor

Universidade Católica Portuguesa

Eligibility Criteria

Inclusion Criteria

  • patients age \> 18 years;
  • American Society of Anaesthesiologists (ASA) status I;
  • no systemic medication or condition known to potentially alter bone metabolism; - absense of acute periodontal condition.

Exclusion Criteria

  • lack of primary stability at implant surgery;
  • need for bone regeneration procedures during surgery;
  • inability to correct place the implant in accordance with the prosthetic requirements.

Outcomes

Primary Outcomes

Marginal bone changes

Time Frame: 60 months

Crestal bone changes that occur around the dental implant

Study Sites (1)

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