Clinical Effects of Hard and Soft Tissue Grafting With Dental Implants
Completed · Not applicable
Conditions studied: Dental Implants
In brief
The study will be done to see if Implant placement and simultaneous grafting using alloderm alone will result in the same facial ridge contour and soft tissue thickness as alloderm plus bovine derived xenograft. Is the facial soft tissue contour and thickness for alloderm plus bovine derived xenograft is significantly increased compared to alloderm alone.
Key facts
- Study ID
- NCT03580811
- Run by
- University of Louisville
- People needed
- 12
- Starts
- 2018-12-04
- Expected to finish
- 2021-04-30
- Last updated by the study team
- 2021-06-03
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Have one edentulous site bordered by 2 teeth in maxillary sites from second premolar to second premolar (maxillary 4 to 13) to receive an implant with simultaneous grafting with an ADMG with or without BDX.
- Healthy persons at least 18 years old.
- Understands and has signed the informed consent.
You may not qualify if…
- Patients with uncontrolled diabetes, immune disease, or any systemic disease that significantly affects the periodontium.
- Previous head and neck radiation.
- Patients who have taken oral bisphosphonates for > 3 years or any IV bisphosphonates.
- Smokers (or other tobacco habits that might interfere with soft tissue healing).
- Patients who need prophylactic antibiotics prior to dental procedures.
- Patients with allergies to any medication or material used in the study, or that would adversely affect study procedures.
- Chemotherapy in the previous 12 months.
- Psychological problems that would interfere with treatment.
- Pregnant subjects will be excluded due to risk of miscarriage
- Patients unable or unwilling to sign the informed consent.
Where it is running
- Graduate Periodontics University of Louisville — Louisville, Kentucky, United States
Full record on ClinicalTrials.gov
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