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Truness of Full Arch Impressions in All on x Cases

Trueness of Full-Arch Impressions Using Photogrammetry, Splinted Digital Scan Bodies Versus Conventional Open-Tray Techniques in the All-on-x Prosthesis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07550725
Enrollment
11
Registered
2026-04-24
Start date
2026-05-01
Completion date
2026-11-01
Last updated
2026-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trueness of Full Arch Implant Prosthesis Impression, Truness of Impression Techniques in All on x Cases

Brief summary

This study aims to compare the trueness and precision of three impression methodologies photogrammetry, digital intraoral scanning with splinted scan bodies, and conventional open tray impressions in the context of the All-on-X treatment concept. This will provide valuable evidence for clinicians considering digital workflows for implant-supported prostheses. Does the use of photogrammetry and digital impression techniques with splinted scan bodies result in improved accuracy in implant position transfer in the All-on-X concept compared to conventional open tray impressions?

Interventions

DEVICEphotogrammetry based full arch impression

use of photogrammetry system to capture the positions of All on X implants digitally without physical impression material. This technique aims to achieve precise measurements and increase patient satisfaction

Digital full-arch impression using splinted scan bodies connected with resin to enhance stability. An intraoral scanner captures the splinted assembly for framework fabrication. Accuracy and patient satisfaction will be evaluated.

Traditional full-arch open-tray impression using polyether or VPS material with splinted impression copings. This serves as the standard comparator for evaluating accuracy and patient satisfaction.

Sponsors

October 6 University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
55 Years to 65 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frame
Accuracy measured using 3D inspection software (Geomagic Control X).Immediately after measurements taking

Secondary

MeasureTime frame
Oral health-related quality of life (OHRQoL), assessed using standardized questionnaires.immediately after measurements taking

Countries

Egypt

Contacts

CONTACThadeer Ali, teaching assistant
hadeeralisoliman5@gmail.com01143252442

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026