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Digital dental implants: can a computer plan match reality?

NCT ID NCT07315607

Knowledge-focused Sponsor: Universidad Complutense de Madrid Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests how accurately a fully digital workflow places dental implants and temporary crowns in one visit. Twenty-seven adults needing a single tooth replacement will receive a digitally planned implant and a prefabricated screw-retained crown. Researchers will compare the planned versus actual positions to see if the digital approach is precise enough for routine use.

What this could mean

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

Active substance
Fully guided implant placement and immediate provisional crown procedure
What this could lead to
If successful, this could confirm that a fully digital workflow produces accurate, same-day dental implants and temporary crowns, reducing the need for adjustments.
What could go wrong
This is a small, early-stage study with only 27 participants, so results may not apply to all patients. The procedure requires high primary stability, which not everyone can achieve.

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 27 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Jan 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: 1. Adults aged 18 years or older. 2. Partially edentulous patients requiring replacement of a single tooth with an immediately loaded dental implant. 3. Patients classified as ASA I or ASA II according to the American Society of Anesthesiologists physical status classification. 4. Patients with clinical conditions allowing immediate implant placement with a minimum primary stability of ≥25 Ncm. 5. Ability to understand the study procedures and provide written informed consent. 6. Willingness to comply with the study protocol and attend required clinical visits. Exclusion Criteria: 1. Patients classified as ASA III or ASA IV, or with uncontrolled systemic conditions that may interfere with study participation. 2. Presence of psychiatric or cognitive disorders that may compromise informed consent or protocol compliance. 3. Inability to comply with the visit schedule or required evaluations. 4. Any other condition that, in the investigator's judgment, could compromise patient safety, protocol adherence, or data validity.

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Conditions

The condition(s) this trial relates to.

Tooth Loss

As listed by the trial registrant

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

Partial edentulism Tooth loss / rehabilitation

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

  • Complutense University of Madrid

    RECRUITING

    Madrid, Madrid, 28040, Spain

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