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Periimplant Bone Changes in Different Abutment Heights and Insertion Timing in Posterior Mandibular Areas

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04340726
Enrollment
Unknown
Registered
2020-04-09
Start date
2015-01-01
Completion date
2015-12-31
Last updated
2020-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Implant Failed

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).

Interventions

PROCEDUREOne time abutment

Sponsors

Universidade Católica Portuguesa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Marginal bone changes60 monthsCrestal bone changes that occur around the dental implant

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026