Multicenter study to evaluate safety and performance of Geistlich Bio-Graft® for horizontal ridge augmentation
Not Applicable
- Conditions
- ridge width insufficient for placement of dental implants
- Registration Number
- DRKS00006107
- Lead Sponsor
- Geistlich Pharma AG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 38
Inclusion Criteria
Need for horizontal ridge augmentation
Exclusion Criteria
general contraindications for oral surgery, diseases or medication interfering with bone metabolism or wound healing, pregnancy and lactation, participation in other clinical trials
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual assessment of the possibility of implant placement after 6 months healing
- Secondary Outcome Measures
Name Time Method assessment of gain in ridge width by means of a caliper after 6 months, assessment of adverse events; soft tissue healing during the study; peri-implant indexes at final visit