Immediate Function of NobelSpeedy Shorty and Brånemark System® Mk III Shorty Implants in Daily Use

NCT02180230•Nobel Biocare

Summary

The aim of this study was to evaluate the 7 mm long implants NobelSpeedy Shorty and Brånemark System Mk III Shorty: by determining the marginal bone remodeling, implant survival rate, soft tissue health and maintenance.

Detailed Description

The primary endpoint was the change in marginal bone levels (in mm) from the time of implant insertion to follow-up visits (3, 6, 12, 36 and 60 months). Further endpoints were: * cumulative survival rates of the implants * soft tissue parameters (papilla index, bleeding on probing) * plaque formation

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•The subjects should have an osseous architecture enough to receive an implant with a diameter of at least 3.75 mm for Brånemark System Mk III Shorty or 4 mm for NobelSpeedy Shorty and a sufficient amount of bone for placing implants with a length of 7 mm.
•The final tightening torque at installation should be 35-45 Ncm without further rotation and should not exceed 45 Ncm.
•The subject as well as the implant site(s) should fulfill criteria for immediate provizionalization.
•Immediate insertion (e.g. placement of the implant immediately after extraction) will not constitute an exclusion criterion.
•The implants site(s) should be free from extraction remnants.
•The subject should be healthy and compliant with good oral hygiene.
•The subject should be available for the 5-year term of the investigation.
•Favorable and stable occlusal relationship

Exclusion Criteria

•Alcohol or drug abuse as noted in patient records or in patient history.
•Health conditions, which do not permit the surgical procedure.
•Reason to believe that the treatment might have a negative effect on the subject's total situation (psychiatric problems), as noted in patient records or in patient history.
•The subject is not able to give her/his informed consent to participate.
•Any disorders in the planned implant area such as previous tumors, chronic bone disease, or previous irradiation.
•Severe bruxism or other destructive habits.

Key Dates

Start Date

October 1, 2007

Primary Completion Date

December 1, 2014

Completion Date

December 1, 2014

Last Updated

April 22, 2016

Enrollment

ACTUAL participants

Conditions

Partial EdentulismComplete Edentulism

Interventions

Shorty implants

DEVICE

In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Using Digital Planning and Guided Surgery

NCT07315607

Partial EdentulismTooth Loss / Rehabilitation

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RECRUITINGNA

Short Implant Versus Crestal Standard Length Implant to Retain Class 1 Removable Partial Denture.

NCT06666595

Bone LossPartial Edentulism Class 1

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 22, 2016Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Immediate Function of NobelSpeedy Shorty and Brånemark System® Mk III Shorty Implants in Daily Use

Inclusion Criteria

Exclusion Criteria

In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Using Digital Planning and Guided Surgery

Short Implant Versus Crestal Standard Length Implant to Retain Class 1 Removable Partial Denture.

Denture Retention of Intra-orally Scanned Versus Extra-orally Scanned Digitally Printed Maxillary Denture in Completely Edentulous Patients

Intraoral vs Extraoral Cementation of Zirconia Bridges on Ti-Bases: Microstrain Evaluation

Post Extraction Wound Healing Evaluation of Immediate Complete Denture Using IPR Scale

Compare CAD/CAM Metallic RPD to Conventional Metallic RPD in Terms of Oral Health Related Quality of Life