DRKS00020222
Recruiting
Phase 4
Guided bone regeneration of peri-implant defects with particulate versus soft-type block bone substitutes. A randomized controlled, single blinded clinical trial - L-Shape
Clinic of Reconstructive DentistryCenter of Dental MedicineUniversity of Zürich0 sites64 target enrollmentJune 15, 2020
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- K00-K14
- Sponsor
- Clinic of Reconstructive DentistryCenter of Dental MedicineUniversity of Zürich
- Enrollment
- 64
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients, in need of at least one implant with an expected peri\-implant bone dehiscence \= 2 mm of apico\-coronal dimension in the maxilla or mandible (excl. molars)
- •\-primary implant stability assessed at implant placement
- •\-no need of soft tissue grafting after implant placement
- •\-tooth extraction performed \= 4 months in advance
- •\-possibly performed soft tissue grafting \= 2 months in advance
- •\-Presence of one adjacent tooth at the implant site;
- •\-Presence of antagonist;
- •\-Adequate oral hygiene (Bleeding on probing \<20%; Plaque index \<20%);
- •\-Capability to comply with the study procedures
- •\-Signed Informed Consent Form
Exclusion Criteria
- •\-Ridge preservation procedure after tooth extraction performed
- •\-Pregnant or lactating women;
- •\-Known or suspected non\-compliance, drug or alcohol abuse
- •\-Smokers (\>10 cigarettes/day including e\-cigarettes)
- •\-Currently taking drugs that influence bone metabolism
- •\-Use of bisphosphonates in the last 4 years
- •\-Systemic or local conditions presenting a contraindication to implant treatment
- •\-History of malignancy, radiotherapy or chemotherapy for malignancy in the past 5 years
Outcomes
Primary Outcomes
Not specified
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