Which dental framework keeps bacteria at bay?
NCT ID NCT07811661
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers compare two materials for making fixed full-arch dental prostheses supported by four implants in people with no natural teeth in the lower jaw. Each participant receives a prosthesis with either a Zantex (fiber-reinforced polymer) or zirconia (ceramic) framework. The study measures bacterial buildup on the framework and checks gum health around the implants over three months. The goal is to see which material may lead to better oral health for this type of dental treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A dental prosthesis framework made from either a fiber-reinforced polymer (Zantex) or zirconia ceramic
- What this could lead to
- If one framework material collects less bacteria and keeps gums healthier, dentists could choose it more often for full-arch implant patients.
- What could go wrong
- This is a small, short study of 14 people followed for three months, so it may not show a clear difference or predict long-term results. Dental implant procedures carry usual risks like infection or implant failure.
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
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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
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About 14 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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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
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40 to 75 years
- Sex
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Anyone
- Healthy volunteers
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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 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: 1. Completely edentulous patients in the mandibular arch. 2. Patients with a completely edentulous maxillary arch rehabilitated with a conventional complete denture. 3. Patients with sufficient mandibular bone volume and quality to allow placement of four implants according to the All-on-Four treatment concept. 4. Patients suitable for placement of two axial anterior implants in the canine regions and two distally tilted posterior implants anterior to the mental foramina. 5. Patients with adequate restorative space to accommodate a full-arch hybrid prosthesis. 6. Patients who are willing and able to maintain adequate oral hygiene and attend all scheduled follow-up appointments. 7. Patients who are willing to participate in the study and sign the informed consent form. \- Exclusion Criteria: * 1\. Patients with systemic conditions that contraindicate implant surgery or may adversely affect osseointegration or wound healing. 2\. Patients receiving medications or undergoing treatments that significantly affect bone metabolism or healing. 3\. Patients with a history of radiotherapy involving the head and neck region that may compromise implant therapy. 4\. Patients with active or uncontrolled periodontal or oral infections. 5. Patients with inadequate mandibular bone volume or unfavorable anatomical conditions that prevent placement of four implants according to the planned All-on-Four protocol without additional augmentation procedures. 6\. Patients with severe parafunctional habits, such as uncontrolled bruxism, that may compromise the prosthetic rehabilitation. 7\. Patients unable or unwilling to maintain appropriate oral hygiene. 8. Patients unable to attend the scheduled follow-up visits. 9. Patients who decline to participate or fail to provide informed consent
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Conditions
The condition(s) this trial relates to.
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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Faculty of Dentistry, Kafrelsheikh University
RECRUITINGKafr ash Shaykh, Kafr el-Sheikh Governorate, 33511, Egypt
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