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Dental Implant Supported Removable Dental Prostheses

NCT03041597 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2017-02-03

No results posted yet for this study

Summary

To prospectively monitor the survival rate of Ankylos® dental implants, comparing delayed versus immediate loading, using abutments with the SynCone® concept for implant-supported detachable dental prosthesis (ISDDP) in the edentulous upper jaw.

Conditions

  • Implant Complication
  • Prosthesis Survival

Interventions

PROCEDURE

placement of implants

surgical procedure and placement of implants

PROCEDURE

immediate loading

cone-anchored implant supported removable dental prostheses placement

PROCEDURE

conventional loading

cone-anchored implant supported removable dental prostheses placement in 3mo

DEVICE

Ankylos implant

Sponsors & Collaborators

  • Dentsply Sirona Implants and Consumables

    collaborator INDUSTRY

  • KU Leuven

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-09-01
Primary Completion
2013-12-31
Completion
2015-12-31

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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 NCT03041597 on ClinicalTrials.gov