Same-Day dental bridges: a trial puts Instant-Load implants to the test
NCT ID NCT00728962
First seen Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time
Summary
This study looks at whether a specific dental implant can hold a temporary bridge right after being placed, so patients don't have to wait months for a permanent restoration. Researchers will follow 75 adults with missing back teeth who need a short bridge. The main question is whether the implant stays stable and fuses with the bone over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a dental implant system (Osseotite Prevail) used for immediate loading with a temporary bridge
- What this could lead to
- If successful, this approach could allow people with missing teeth to receive a functional temporary bridge on the same day as implant surgery, reducing wait time.
- What could go wrong
- This is an observational study without a control group, so results may not prove superiority over standard approaches. Implant failure or bone loss remain possible risks.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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75 people
The number who actually took part.
- Start date
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Mar 2005
- Finished
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Oct 2009
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
These will be patients who are otherwise seeking dental implant therapy and belong to the study centers' standard patient population.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 of either sex and of any race, 18 years of age or older * patients for whom the decision has already been made to use dental implants for treating partial edentulism in the posterior mandible or maxilla using a short span fixed prosthesis of two to four units * patients must be physically able to tolerate conventional surgical and restorative procedures * requirements for implant placement include: at least 1mm bone will be available at the buccal and lingual aspect of the implant and at least 1mm of bone below the apex * patients must agree to return to the clinic for each study follow-up visit * requirements for prosthetic fabrication include: bone width at least 6mm and a bone height of at least 11mm Exclusion Criteria: * patients with active infection or severe inflammation in the areas intended for implant placement * patients with a \>10 cigarettes / day smoking habit * patients with uncontrolled diabetes or metabolic bone disease * patients with a history of therapeutic radiation to the head * patients in need of bone grafting at the site of the intended study implant; if at the time of surgery some lateral voids need to be filled this is acceptable and does not exclude the patient from the analysis * patients who are known to be pregnant * patients with para-functional habits with evidence of severe bruxing or clenching * placement of implants into sites with less than sixteen weeks of post-extraction healing; for 3-4 unit cases one implant site may have less than sixteen weeks of healing prior to implant placement * type III or IV bone characteristics of the intended implant sites * inter-arch distance of less than 7mm (planned location of implant seating platform to the apposing occlusal landmark)
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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 Southern California
Los Angeles, California, 90089, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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