CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 69 enrolled
Drug / intervention
Inmediate abutment heightdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04230837
NCT04230837N/ACompleted

Marginal Bone Levels Around Implants With Definitive Abutments Of One and Three Millimeters: A One Year Of Follow Up Randomized Clinical Trial

Universitat Internacional de Catalunya·interventional·Posted Jan 18, 2020·Updated Jan 18, 2020

In Brief

A clinical study evaluating Inmediate abutment height for Implant Site Reaction. Completed, enrolled 69 participants across 1 site.

Detailed Summary

The aim of the present study was to evaluate the peri-implant crestal bone level around implants placed 1.5 mm subcrestally, with a 1 mm or 3 mm definitive abutment height at the time of implant placement after 1 year. Patients were selected from the Department of Periodontology at Universitat Internacional de Catalunya. X-rays were taken at the time of implant placement, 8-12 weeks after placement, after screwing the provisional rehabilitation and at 12 months. An examiner indicated the crestal marginal bone level, the marginal bone level of the implant, and the marginal bone level of the abutment . The examiner, independent to the study, carried out the radiographic analysis using the Image J software on periapical radiographs.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJan 18, 2020
Enrollment StartJan 1, 2017
Primary CompletionJul 1, 2018
Study CompletionJul 1, 2019
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 6.5 years ago

Interventions

Inmediate abutment heightdevice

The placement of the implant was done following the manufacturing protocol and using a surgical guide according to the radiological guide previously used. At this time, the Permanent® abutment of 1 or 3 mm was chosen randomly and was placed at 35 Ncm.