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New bone graft could improve dental implant success after tooth extraction

NCT ID NCT06740110

Disease control Sponsor: Medical Inventi S.A. Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares a new bone graft material to standard care for preserving bone after tooth extraction. About 82 adults who need socket preservation will be randomly assigned to receive either the new material or the usual treatment. The main goal is to measure how much new bone forms using microscopic analysis, with safety also tracked.

What this could mean

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

Active substance
bone graft material (investigational medical device)
What this could lead to
If successful, this could provide a better option for preserving bone after tooth extraction, potentially improving outcomes for future dental implants.
What could go wrong
This is an early-stage study with only 82 participants, so results may not apply to everyone. The new material may not perform better than standard care, and there are typical surgical risks like infection or poor healing.

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 82 people

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

Started

Oct 2025

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

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.

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: * Patients over 18 years old with full legal capacity, male and female; * Patients with ability to understand the proposed surgical treatment and to understand and sign the informed consent; * Patients who are willing and able to comply with scheduled visits, treatment and other trial procedures; * Patients who respect the follow-up recalls. Exclusion Criteria: * Presence of bone lesions; * Patients with alcohol or substance abuse; * Patients with smoking habits (more than 10 cigarettes per day); * Patients presenting physical and/or mental handicap that impede an adequate oral hygiene; * Pregnant or breast feeding women; * Patients currently participating in any other clinical investigation.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Socket preservation

Contacts and locations

Locations

  • Indywidualna Praktyka Stomatologiczna Marek Śmielecki

    Gniezno, 62-200, Poland

  • Medicare

    Mińsk Mazowiecki, 05-300, Poland

  • Rafał Dobrakowski Dentysta

    Wroclaw, 53-030, Poland

  • Stomatologia Niteckie Sp. z o.o.

    Tychy, 43-100, Poland

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