Clinical Assessment of Dental Implant

NACompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

February 2, 2015

Primary Completion Date

March 31, 2016

Study Completion Date

June 30, 2019

Conditions
Tooth Loss
Interventions
DEVICE

MIS Implants

The implantation procedure will be carried out according to a standard surgical protocol, and according the manufacture protocol. Patient will be randomly assigned to one of the two groups after flap opening. The implant stability will be measured using the wench key and recorded in N/cm. The implants will be covered with healing abutments for trans-gingival healing for a period of 4 months. The area will be sutured with thin nylon sutures for a primary passive fit closure. Immediately after the surgery the patient will perform a CBCT of the treated area with a cotton roll on the buccal side in order to be able to evaluate the buccal soft tissue thickness.

Trial Locations (1)

4000

CHU de Liège - Service de Médecine Dentaire, Liège

Sponsors
All Listed Sponsors
collaborator

MIS Implant Technologies, Ltd

INDUSTRY

lead

University of Liege

OTHER