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NCT03149172 · ClinicalTrials.gov registry record · NA
Comparison of Post Tooth Extraction Healing Using Different Xenograft Materials
A NA study, sponsored by Tufts University.
- Completed
- Registry status
- NA
- Development phase
- 25
- Enrollment target
NCT03149172 is a NA study that has completed, run by Tufts University. The registered enrollment target is 25 participants.
The verdict
NCT03149172, a NA study, has completed, sponsored by Tufts University.
- COMPLETED
- Registry status
- NA
- Development phase
- 25 participants
- Enrollment target
Study Summary
The purpose of this pilot study is to conduct a interventional prospective clinical trial to evaluate the efficacy of three different xenografts for ridge preservation by comparing the quality of newly formed bone using histomorphometric and micro CT analysis.The three xenograft materials under investigation are Bio-Oss® (bovine derived xenograft), Equimatrix® (equine derived xenograft), and Endobon® (bovine derived xenograft). There are no prospective studies comparing the effectiveness of these three materials, Bio-Oss®, Endobon® and Equimatrix®, when placed in extraction sockets. Participants will be recruited from patients in the TUSDM clinics that require extraction of single rooted non-molar tooth and are treatment planned to receive dental implants in the future. Participants will be randomized to receive one of the three xenograft materials after tooth extraction. The percentage of newly formed bone and bone density will be compared between the three materials 4-6 months after ridge preservation.
Interventions
- DEVICE Bio-Oss®
- DEVICE Equimatrix®
- DEVICE Endobon®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2014-10-20 |
| Est. Completion | 2016-12-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03149172
The ClinicalTrials.gov registry entry for NCT03149172 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts University, which has 163 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Bio-Oss® is the first listed.
NCT03149172 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03149172 about?
NCT03149172 is a clinical study titled "Comparison of Post Tooth Extraction Healing Using Different Xenograft Materials". The purpose of this pilot study is to conduct a interventional prospective clinical trial to evaluate the efficacy of three different xenografts for ridge preservation by comparing the quality of newly formed bone using histomorphometric and micro CT analysis.The three xenograft materials under inve...
What is the current status of trial NCT03149172?
This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2014-10-20. Estimated completion is 2016-12-07.
What interventions are being tested in trial NCT03149172?
The interventions under investigation include: Bio-Oss® (DEVICE), Equimatrix® (DEVICE), Endobon® (DEVICE).
Who is sponsoring clinical trial NCT03149172?
This trial is sponsored by Tufts University, which has 163 total clinical trials registered on ClinicalTrials.gov.
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