New drill technique may eliminate need for bone grafts in dental implants
NCT ID NCT07436533
First seen Jun 26, 2026 · Last updated Aug 12, 2026 · Updated 4 times
Summary
This study tests a special drilling technique called osseodensification to widen narrow jawbone so dental implants can be placed without extra bone grafting. Thirty adults with healed tooth sockets and narrow ridges will have their bone width measured before and after the procedure. The goal is to see how much the bone expands using this method alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Densah burs used in osseodensification drilling technique
- What this could lead to
- If successful, this technique could allow dental implant placement in narrow jawbones without additional bone grafting, simplifying the procedure.
- What could go wrong
- This is a small, early study with only 30 participants and no comparison group. Results may not apply to all patients or jaw types.
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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35 people
The number who actually took part.
- Started
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Feb 2025
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- 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 80 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: * Adults aged 18 years or older and within the upper age limit specified in the final ethics-approved protocol. * Healed edentulous sites involving single or multiple missing teeth in the maxillary or mandibular arches. * A post-extraction healing period of at least 6 months before implant placement. * Adequate vertical bone dimensions for dental implant placement, as assessed using CBCT. * Absence of active local infection or pathological lesions at the proposed implant site. * Clinical suitability for dental implant placement and osseodensification-assisted osteotomy preparation. * Ability and willingness to provide informed consent and attend the scheduled follow-up visits. * Maintenance of acceptable oral hygiene. * Alveolar ridge width of ≤8 mm at the crestal level, measured buccolingually, and considered to require horizontal expansion during implant-site preparation. * Implant sites classified as Misch D1-D4 according to the protocol-specified bone-quality assessment. Exclusion Criteria: * Acute or chronic infection or a pathological condition at the proposed implant site. * Severe buccal plate undercut or ridge concavity that precluded safe implant-site preparation. * Insufficient vertical bone height for the planned dental implant. * Inadequate interarch distance for implant-supported rehabilitation. * Severe parafunctional habits, including clinically significant bruxism or clenching. * Heavy smoking, defined as more than 10 cigarettes per day. * Use of medications considered likely to compromise bone healing according to the approved protocol, including relevant corticosteroid or antiresorptive therapy. * Uncontrolled systemic disease or a medical condition that could materially affect surgical healing or implant treatment. * History of radiotherapy to the head and neck or chemotherapy within the preceding 5 years. * Current pregnancy at the time of the surgical procedure. * Inability or unwillingness to provide informed consent or attend the required follow-up visits
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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
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60 Meters St., Madbah, University of Science and Technology
Sanaa, S, (15201 - 13064), Yemen
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Other studies related to the condition(s) this trial covers.
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