3D Facial Scanning in Full-Arch Implant Prosthodontics: Time Efficiency and Patient Satisfaction (NCT07751900) | Clinical Trial Compass
CompletedNot Applicable
3D Facial Scanning in Full-Arch Implant Prosthodontics: Time Efficiency and Patient Satisfaction
Egypt22 participantsStarted 2024-10-31
Plain-language summary
This study compares two ways of planning the bite (jaw-relation) stage of full-arch, implant-supported dental prosthesis treatment: a standard digital approach, and the same approach with the addition of 3D facial scanning, which lets the dental team plan the new teeth against a scan of the patient's own face. The study measured how patients felt about their treatment using a validated questionnaire, and also tracked how many clinic visits and adjustments each approach needed. Twenty-two patients took part, randomly assigned to one of the two approaches.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adults (≥18 years) indicated for full-arch maxillary implant-supported fixed prosthetic rehabilitation
* Completion of the surgical phase with stable implant osseointegration
* Presence of healthy peri-implant soft tissues
* Adequate oral hygiene status
* Sufficient bone and soft-tissue conditions compatible with full-arch prosthetic rehabilitation
* Ability to comply with all scheduled follow-up visits
* Capacity to maintain natural head position during facial scanning procedures
* Absence of significant gag reflex interfering with scanning/impression procedures
* Ability to communicate effectively and complete questionnaires
* Provision of written informed consent
* Physically and psychologically fit for the planned treatment
Exclusion Criteria:
* Severe skeletal or orthognathic discrepancies
* History of significant facial trauma or surgery affecting facial symmetry
* Prior maxillofacial pathology affecting the surgical/prosthetic site
* Uncontrolled systemic diseases affecting healing or treatment tolerance
* Use of medications that alter osseointegration or facial soft tissues
* Active oral or peri-implant infection
* Neuromuscular disorders or temporomandibular joint dysfunction affecting jaw positioning
* Conditions affecting the ability to maintain stable head position for scanning
* Severe psychomotor limitations
* Known hypersensitivity to materials used in bite registration or prosthesis fabrication
* Inability or unwillingness to provide i…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Total Oral Health Impact Profile-14 (OHIP-14) Score at Trial-Wear Timepoint
Timeframe: 4 weeks
2
Total Oral Health Impact Profile-14 (OHIP-14) Score at Post-Delivery Timepoint