Titanium versus Nano-Carbon CAD/CAM frameworks for All-on-4 implant supported hybrid prosthesis. a study of peri-implant tissue changes and prosthetic complications
NCT ID NCT07812363
First seen Sep 10, 2026 ยท Last updated Sep 10, 2026
Summary
This clinical study compares two CAD/CAM framework materials, titanium and nano-carbon fiber-reinforced composite, used in mandibular All-on-4 implant-supported hybrid prostheses. Ten completely edentulous patients are randomly allocated into two equal groups. The study evaluates peri-implant soft tissue health, changes in marginal bone levels,and prosthetic complications over an 12-month follow-up period.
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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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10 people
The number who actually took part.
- Started
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May 2024
- Finished
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Aug 2026
- 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * \* Completely edentulous patients requiring mandibular implant-supported rehabilitation. * Adequate bone quantity and quality in the mandibular interforaminal region for implant placement. * Adequate restorative space for an implant-supported hybrid prosthesis. * Healthy oral mucosa and acceptable oral hygiene. * Patients medically fit to undergo implant surgery. * Ability and willingness to attend the scheduled follow-up visits and provide informed consent. Exclusion Criteria: * Systemic conditions or medical contraindications that could interfere with implant surgery or healing. * History of radiotherapy to the head and neck region. * Smoking. * Alcohol abuse. * Bruxism or clenching habits. * Any local condition that could compromise implant placement or the planned prosthetic rehabilitation.
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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.
Contacts and locations
Locations
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Faculty of Dentistry, Mansoura University
Al Mansurah, Dakahlia Governorate, Egypt
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Other studies related to the condition(s) this trial covers.
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