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NCT Number: NCT07235072

Passive Fit and Time Efficiency in All On-X Implants Protocols Using Photogrammetry, Splinted Scan Bodies, and Conventional Impression Technique

compare the passive fit of three impression techniques: photogrammetry, intraoral digital scanning with splinted scan bodies, and the conventional open-tray impression technique, within the context of the All-on-X treatment concept. This comparison is expected to provide valuable clinical evidence to support clinicians in making informed decisions when considering the adoption of digital alternatives to conventional methods.

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Key information

Age range

45 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

For edentulous patients undergoing full-arch rehabilitation, the All-on-X treatment approach has proven to be a very successful option, providing enhanced function, aesthetics, and patient satisfaction. Achieving passive fit, which reduces mechanical stress on implants and prosthetic components and reduces the possibility of problems such screw loosening, fracture, or marginal bone loss, is crucial to the long-term effectiveness of implant-supported prostheses. Passive fit has traditionally been evaluated after prostheses are fabricated using traditional open-tray impression techniques, which are regarded as the gold standard because of their great precision and dependability. These approaches, however, are challenging, technique-specific, and susceptible to human mistake or material deformation. Other methods include digital intraoral scanning with splinted scan bodies and photogrammetry have become more appreciated due to the quick development of digital dentistry. Potential advantages of these digital workflows include quicker digital data transfer to the lab, less chairside time, and improved patient comfort. In the context of the All-on-X procedure, there is still no clinical data comparing the accuracy especially passive fit and time efficiency of these more recent methods with traditional impressions, despite these benefits. Thus, the purpose of this study is to compare the time efficiency and passive fit of three impression techniques: traditional open-tray impressions, digital intraoral scanning with splinted scan bodies, and photogrammetry. The findings will provide clinicians with evidence-based insights into whether digital alternatives can match or surpass traditional techniques in terms of accuracy and workflow efficiency, ultimately supporting the transition toward more modern, streamlined protocols in implant prosthodontics.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Photogrammetry-Based Full-Arch Impression

Device

Use of a photogrammetry system to capture the positions of All-on-X implants digitally without physical impression materials. The technique aims to achieve precise passive fit and reduce chairside working time. Measurements of passive fit discrepancy and total procedure time will be recorded

Digital Impression Using Splinted Scan Bodies

Device

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

Conventional Open-Tray Implant Impression

Procedure

Traditional full-arch open-tray impression using polyether or VPS material with splinted impression copings. This serves as the standard comparator for evaluating passive fit and procedure duration

Primary outcomes

  1. Passive fit measured using 3D inspection software (Geomagic Control X)

    Time frame: Immediately after framework verification

Secondary outcomes

  1. Time efficiency, assessed using stop watch and measured by seconds.

    Time frame: During impression procedure

Study contacts

Contact information is provided by the study sponsor or research team.

Mohammed Fathy Ghobashy, Bachelor of Dental Surgery

CONTACT

[email protected]

00201099632823

Sponsors and collaborators

Lead sponsor

October 6 University

Other

Registry information

Official study title

Comparative Analysis of Passive Fit and Time Efficiency in Allon-X Implants Protocols Using Photogrammetry, Splinted Scan Bodies, and Conventional Impression Technique

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Nov 19, 2025
Registry last updated
Nov 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.