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Dental implant study seeks best fit method

NCT ID NCT07235072

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares three methods for taking dental impressions in people getting full-arch implants (All-on-X). The goal is to see which method gives the most accurate fit and is fastest. Fourteen adults aged 45-65 will be enrolled to help dentists choose the best technique.

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 14 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Oct 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

45 to 65 years

Sex

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

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

Inclusion Criteria: Adults aged 45-65 years. Fully edentulous or partially edentulous maxilla requiring full-arch rehabilitation. Sufficient maxillary bone volume to support at least four implants according to the All-on-X protocol. Systemically healthy patients with no contraindications to dental implant surgery (ASA I-II classification). Demonstrated ability to maintain adequate oral hygiene. Willingness to participate in the study and comply with follow-up visits and required maintenance protocols. Patients seeking a fixed, implant-supported prosthesis for the maxilla due to missing teeth and inability to use removable prostheses effectively. Acceptable radiographic findings with no signs of pathology, infection, or significant anatomical limitations. Exclusion Criteria: Uncontrolled systemic diseases (e.g., uncontrolled diabetes, osteoporosis, immunosuppressive disorders) History of radiation therapy to the head and neck region Active periodontal disease or untreated caries Maxillary cysts, tumors, or pathologies Poor oral hygiene or inability to maintain postoperative care Insufficient bone volume for All-on-X without extensive grafting Maxillary sinus pathology or oroantral fistula Psychiatric illness or cognitive impairment affecting compliance Bruxism or parafunctional habits Pregnant or lactating women History of implant failure or titanium allergy Use of bisphosphonates or antiresorptive medications Heavy smoking (\>10 cigarettes/day) Inability or unwillingness to attend follow-up visits Diagnosed or symptomatic temporomandibular joint disorders (pain, clicking, locking, limited opening)

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As listed by the trial registrant

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How to take part

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  1. The official record

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  2. A doctor treating you

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