Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Dentsply Sirona Implants and Consumables
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Provision of informed consent
Aged 18-75 years at enrolment
A lingual-buccal difference in bone height between 2.0-5.0 mm at the implant site
History of edentulism in the study area of at least 3 months
Presence of alveolar bone crest dimensions judged by the investigator to allow ≥1mm of bone circumferential to the implant after implant placement.
In need for a single implant replacing a missing tooth in any location with an adjacent natural tooth mesially, and an adjacent natural tooth or edentulous space distally to the planned implant position (i.e. no existing or planned implant adjacent to the planned study implant position)
Deemed by the investigator as likely to present an initially stable implant situation
You may not be if
Uncontrolled pathological processes in the oral cavity
Known or suspected current malignancy
History of radiation therapy in the head and neck region
History of chemotherapy within 5 years prior to surgery
Systemic or local disease or condition that would compromise post-operative healing and/or osseointegration
Uncontrolled diabetes mellitus
Corticosteroids or any other medication that would compromise post-operative healing and/or osseointegration
Smoking more than 10 cigarettes per day
Present alcohol and/or drug abuse
Current need for bone grafting in the planned implant area
Previous enrolment in the present study
Simultaneous participation in another clinical study or participation in a clinical study during the last 6 months
Involvement in the planning and conduct of the study (applies to both Sponsor staff or staff at the study site)
Unlikely to be able to comply with study procedures, as judged by the investigator
