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CF41102 5-year Clinical Evaluation of Conelog® Implant With 7 mm Length

NCT03558347 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-03-17

No results posted yet for this study

Summary

The objective of this prospective, randomized, pilot study is to determine whether the Conelog® connection is suitable for splinted/non-splinted cemented crowns in the chewing centre (focus only on implant-abutment connection) and whether implants with the Conelog® connection and a length of 7mm are suitable for use in the molar region of the lower jaw.

Conditions

  • Dental Implants
  • Partial Edentulism

Interventions

DEVICE

short implants with splinted crowns

7 mm short implants (CONELOG® Implant System), individualized titanium abutments, splinted lithium disilicate crowns

DEVICE

short implants with non-splinted crowns

7 mm short implants (CONELOG® Implant System), individualized titanium abutments, non-splinted lithium disilicate crowns

Sponsors & Collaborators

  • Camlog Oral Reconstruction Foundation

    collaborator OTHER

  • RWTH Aachen University

    lead OTHER

Principal Investigators

  • Stefan Wolfart, Prof. Dr. · University Hospital, Aachen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-01
Primary Completion
2016-09-27
Completion
2021-09-27

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03558347 on ClinicalTrials.gov