Clinical trial Recruiting at 1 site Interventional Ages 35 to 70

Passive Fit of Implant-Supported Frameworks Using Digital vs Conventional Impressions

Official title: Passive Fit Evaluation of Full-Arch Implant-supported Frameworks Using Digital and Conventional Impression Techniques: Crossover Study

Run by Mansoura University · NCT07778199 · Data updated 2026-11-12

This study tests whether three impression methods can produce a passively fitting full-arch mandibular implant framework for edentulous patients.

Quick facts

Study typeInterventional
Ages35 Years to 70 Years
SexAll
Enrollment8 (estimated)
SponsorMansoura University
Academic / other
Locations1 site (Al Mansurah, Dakahlia Governorate)
StatusRecruiting
StartedJanuary 25, 2026
Main results expectedOctober 25, 2026
Study endsJanuary 25, 2027
Registry record updatedAugust 21, 2026
Trial IDNCT07778199 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 35-70 who are fully edentulous and require a four-implant-supported mandibular fixed prosthesis, with adequate bone and ability to participate in all three Impression workflows.

Probably not a fit

Patients with systemic conditions affecting healing, active oral infection, severe bruxism, or inability to complete all three impression procedures may not benefit from the study outcomes.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized crossover trial compares the passive fit of complete-arch mandibular implant-supported frameworks fabricated from three impression techniques: IO-Connect non-calibrated digital splinted scan bodies, a Reverse Scan Body digital method, and conventional splinted open-tray impressions. Eight completely edentulous participants with at least four mandibular implants will receive four implants and undergo all three impression workflows in a randomized sequence. The fit will be assessed clinically with the Sheffield one-screw test and radiographically with parallel periapical radiographs to detect microgaps at the implant-framework interface. The study addresses whether digital workflows can achieve equivalent passive fit to conventional methods in full-arch prostheses.

Why it matters

Potential benefit: If successful, digital impression techniques may simplify workflows and reduce chair time while maintaining a passive fit for full-arch implant prostheses.

How similar studies have gone: Prior studies have explored digital vs conventional impressions for implant prostheses, but direct, multi-technique, crossover comparisons for complete-arch frameworks are limited and this design adds novel assessment of IO-Connect and Reverse Scan Body methods.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Completely edentulous patients requiring full-arch implant-supported fixed prosthesis
* Age 35-70 years
* Adequate mandibular bone to place at least four implants without major grafting
* Ability to undergo digital scanning and radiographic evaluation
* Signed informed consent

Exclusion Criteria:

* Systemic conditions affecting healing (uncontrolled diabetes, immunosuppression)
* History of head/neck radiotherapy or bisphosphonate therapy
* Active oral infection or severe bruxism
* Strong gag reflex preventing accurate scanning
* Poor compliance or unwillingness to attend follow-up visits

Where it's running

  • Faculty of Dentistry, Mansoura University
    Al Mansurah, Dakahlia Governorate, Egypt
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.