Prospective Evaluation of Anorganic Bovine Bone Mineral Versus Calcium Phosphosilicate Alloplastic Bone Putty in Direct Sinus Augmentation: a Spilt-mouth Study
Completed · Not applicable
Conditions studied: Sinus Floor Augmentation, Maxillary Sinus
In brief
The purpose of this split-mouth clinical study is to evaluate the clinical, radiographic and histological outcomes of lateral window sinus augmentation with a bovine xenograft or a CPS putty bone substitute in posterior maxillary sites and the survival of implants placed in these sites following healing.
Key facts
- Study ID
- NCT01942304
- Run by
- University of Minnesota
- People needed
- 12
- Starts
- 2013-10-01
- Expected to finish
- 2019-05-31
- Last updated by the study team
- 2019-11-01
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patients with non-contributory medical history that will present for bilateral sinus lift surgery prior to implant placement
You may not qualify if…
- Patients that will not agree to participate in this study or sign the consent form
- More than 8mm of residual bone height at the implant site
- Subjects smoking more than 10 cigarettes per day
- History of acute sinus infection
- History of prior maxillary sinus surgery (Caldwell-Luc, direct or indirect sinus lift, etc)
- Medications that affect bone healing (chronic steroid regimen, oral or IV bisphosphonates, etc.)
- Patients allergic to bovine derivatives
- Patients who are a carrier of transmissible disease(s) that may unnecessarily expose laboratory personnel to risks
- Females during pregnancy or lactation or females that plan to become pregnant in the following year (pregnancy test prior to enrollment)
Where it is running
- Advanced Education in Periodontology Clinic, Dental School, University of Minnesota — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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