Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Which dental implant surface keeps bone strongest? new trial aims to find out

NCT ID NCT06086873

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests three different dental implant surfaces to see which one best preserves the bone around the implant and gives the best look. Thirty-nine adults needing a tooth replaced will get one of the three implant types. Researchers will measure bone changes and patient satisfaction one year after the implant is placed.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
dental implant with different surface textures (NGA, BLX, TLX)
What this could lead to
If successful, this could help dentists choose the best implant surface to keep bone stable and improve long-term appearance.
What could go wrong
This is a small, early-stage study with only 39 people, so results may not apply to everyone. It looks at bone changes and appearance, not cure or disease treatment.

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 39 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2023

Expected to finish

Mar 2027

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age: over 18 years old, * Gender: male and female. * Patient must be able and willing to follow study procedures and instructions and have capacity to provide informed consent. * Patient must require tooth extraction of a maxillary first premolar or single-rooted anterior tooth as the result of caries, endodontic failure or trauma * The extraction site must have adjacent teeth present. * Adjacent teeth with no evidence of interdental bone loss Exclusion Criteria: * Systemic disease that can interfere with dental implant therapy (e.g. uncontrolled diabetes) * 2 adjacent teeth requiring extraction * Greater than one wall of the socket missing - assessed at time of extraction * Any contraindications for oral surgical procedures * Any known systemic disease affecting bone metabolism (e.g. Cushing's syndrome, Crohn's disease, rheumatoid arthritis, osteoporosis, diabetes type I and uncontrolled diabetes type II), systemic infections or recent surgical procedures within 30 days of study initiation; * Chronic treatment (i.e., 2 weeks or more) with any medication known to affect oral status (e.g., phenytoin, dihydropyridine, calcium antagonists and cyclosporine) or bone metabolism (e.g. bisphosphonates, hormone replacement therapy, immunosuppressants) within 1 month before baseline visit; * HIV or viral hepatitis; * Physical handicaps that would interfere with the ability to perform adequate oral hygiene; * History of local irradiation therapy in the head-neck region * Mucosal diseases (e.g. erosive lichen planus) * Current untreated periodontitis or gingivitis. In particular probing depths of \>4mm on one of the teeth immediately adjacent to the extraction site * Untreated acute endodontic lesions * Current smokers (have smoked within 3 months of study onset) * Any known systemic disease affecting bone metabolism (e.g. Cushing's syndrome, Crohn's disease, rheumatoid arthritis, osteoporosis, diabetes type I and uncontrolled diabetes type II), systemic infections or recent surgical procedures within 30 days of study initiation; * Self-reported alcoholism or chronic drug abuse; * Patients suffering from a known psychological disorder or with limited mental capacity or language skills such that study information could not be understood, * Non-compliant patients, vulnerable individuals or those unable to understand written or verbal communication and give consent. * Pregnant or breastfeeding patients * Involvement in current research or recent involvement in any research prior to recruitment * Full-mouth bleeding (BOP) and plaque (PI) scores \>30% or sites with periodontal pocket depth \>5 mm at the completion of the pre-treatment phase.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Dental implant are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Royal London Dental Institute

    RECRUITING

    London, E1 1BB, United Kingdom

More trials for these conditions

Other studies related to the condition(s) this trial covers.