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A Comparison of Bone Formation With Three Different Bone Graft Materials Following Sinus Graft
NCT01911819 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to compare new bone formation following bone graft in sinus using three different commercially available bone graft materials. The study hypothesis is that there is no difference in new bone formation among three bone graft materials under microscope.
Conditions Studied
Interventions
- PROCEDURE Sinus augmentation
- DRUG Equimatrix
- DRUG OSSIF-i sem
- DRUG Bio-oss
Study Locations (1)
California
- Loma Linda University School of Dentistry — Loma Linda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2013-12 |
| Est. Completion | 2016-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01911819
The ClinicalTrials.gov registry entry for NCT01911819 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Loma Linda University, which has 191 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Inadequate Bone Height in Maxillary Posterior Area appearing as the primary indexed condition, and to 4 interventions — of which Sinus augmentation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01911819 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01911819 about?
NCT01911819 is a clinical study titled "A Comparison of Bone Formation With Three Different Bone Graft Materials Following Sinus Graft". The purpose of this study is to compare new bone formation following bone graft in sinus using three different commercially available bone graft materials. The study hypothesis is that there is no difference in new bone formation among three bone graft materials under microscope.
What is the current status of trial NCT01911819?
This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2013-12. Estimated completion is 2016-06.
What conditions does trial NCT01911819 study?
This clinical trial studies the following conditions: Inadequate Bone Height in Maxillary Posterior Area. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01911819?
The interventions under investigation include: Sinus augmentation (PROCEDURE), Equimatrix (DRUG), OSSIF-i sem (DRUG), Bio-oss (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01911819?
This trial is sponsored by Loma Linda University, which has 191 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01911819 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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