Can a plasma boost make dental implants hold stronger?
NCT ID NCT07744776
First seen Aug 04, 2026 · Last updated Sep 09, 2026 · Updated 2 times
Summary
This trial compares different dental implant designs and surface treatments to see how they affect early stability in the jawbone. Fifty adults needing a single implant in the lower back jaw will be randomly assigned to one of five implant types, including some with a special plasma-activated surface. The study measures how tightly the implant fits at placement and how stability changes over six weeks, aiming to find which combination offers the best start for long-term success.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dental implants with different macro-designs and surface treatments, including chairside plasma activation (XActive) and manufacturer surfaces (SLA, SLActive, Xpeed).
- What this could lead to
- If successful, this could help dentists choose implant designs and surface treatments that improve early stability, potentially reducing implant failure and speeding up recovery.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. The findings might not apply to all patients or implant types, and the treatments are only tested for early stability, not long-term success.
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
-
About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2026
- Expected to finish
-
Nov 2026
An estimate. End dates often move.
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Age ≥ 18 years * Requiring a dental implant in a healed mandibular molar site (≥ 3 months post-extraction) * Site anatomy suitable for placement of a 4.1 × 10 mm implant * Bleeding on probing \< 20% * Plaque index \< 25% Exclusion Criteria: * Smoking ≥ 10 cigarettes/day * History of uncontrolled periodontitis * Uncontrolled diabetes * Alcoholism * Use of medication known to impair bone healing
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Dental implant macrodesign are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Dantu implantologijos centras
RECRUITINGVilnius, 08216, Lithuania