Dental bone graft showdown: fibers vs particles in sinus lifts
NCT ID NCT06173791
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether adding bone graft fibers instead of particles to a standard bone substitute leads to more new bone growth in the upper jaw. Twenty-six adults needing sinus augmentation before dental implants received both types of graft material. Researchers measured bone formation six months later using tissue samples and scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Demineralized freeze-dried bone allograft (DFDBA) fibers and particles, combined with deproteinized bovine bone mineral (DBBM)
- What this could lead to
- If fibers work better, dentists may have a new option to improve bone growth for dental implants in the upper jaw.
- What could go wrong
- This is a small, completed study with only 26 participants, so results may not apply to everyone. The difference between fibers and particles might be small or not clinically meaningful.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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26 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 89 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients between age 18 and 89 * Patients needing sinus augmentation to support implant placement in the posterior maxilla * Patients must be nonsmokers, former smokers, or current smokers who smoke \<10 cigarettes per day, by self-report * Female patients who have undergone a hysterectomy, tubal ligation, or menopause, and non- pregnant women of child-bearing potential. Exclusion Criteria: * Patients who disclose that they will not be able to cooperate with the follow-up schedule. * Patients who are mentally incompetent, prisoners, or pregnant (as obtained via chart review or self-report) * Pregnant women or women intending to become pregnant during study period * Smokers who smoke \> 10 cigarettes per day
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229, United States
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