Guided bone regeneration for peri-implant defects using particulated and block bone substitute. A randomized controlled clinical study (block vs granulat)
Not Applicable
- Conditions
- Patients in need of implant therapy with an expected peri-implant bone defect in the maxilla or mandible.K08.1Loss of teeth due to accident, extraction or local periodontal disease
- Registration Number
- DRKS00005803
- Lead Sponsor
- niversity of Zurich, Center of Dental Medicine, Clinic of Reconstructive Dentistry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 29
Inclusion Criteria
1) at least 18 years old
2) in need of at least one implant with an expected peri-implant bone dehiscence in the maxilla or mandible
3) primary stability of the implant must be achieved.
4) Following implant placement, a type defect of 3 mm or more must be present for inclusion.
Exclusion Criteria
-Pregnant
-Heavy smokers (>10 cigarettes per day)
-Pipe and cigar smokers
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method