Clinical trial Recruiting at 1 site Interventional Ages 35 to 60

Accuracy of the Calibrated Framework for Full-Arch Implant Impressions in Edentulous Patients

Official title: Accuracy of the Calibrated Framework for Intraoral Full-Arch Scanning Compared With Conventional Splinted Open-Tray Impression in Edentulous Patients: A Crossover Clinical Trial

Run by Mansoura University · NCT07858682 · Data updated 2026-11-12

This study tests whether digital scanning with a calibrated framework can match the accuracy of traditional splinted impressions for full-arch dental implants in completely toothless patients.

Quick facts

Study typeInterventional
Ages35 Years to 60 Years
SexAll
Enrollment20 (estimated)
SponsorMansoura University
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Al Mansurah)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedFebruary 1, 2027
Study endsApril 1, 2027
Registry record updatedOctober 5, 2026
Trial IDNCT07858682 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older who are completely edentulous in the maxilla and mandible, have sufficient bone and interarch space, good oral hygiene, and no uncontrolled systemic diseases.

Probably not a fit

Patients with poor saliva management, severe parafunctions, or conditions compromising implant accuracy may not experience benefit.

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

What this trial studies

In this crossover study, researchers compare two implant impression methods in adults who are fully edentulous: a conventional splinted open-tray impression and an intraoral digital scan using a calibrated framework. Each participant receives both techniques after implant placement, enabling within-subject comparison of accuracy. The resulting STL files will be superimposed to evaluate how well each method transfers implant positions and supports a passive prosthetic fit. The goal is to determine if digital scanning with a calibrated framework can provide comparable or superior accuracy while potentially reducing technique sensitivity and time. This work addresses the risk of misfit-related complications in full-arch implant rehabilitation.

Why it matters

Potential benefit: If successful, patients could benefit from faster, potentially safer, and more convenient impression methods with reliable prosthetic fit.

How similar studies have gone: Previous work suggests digital scanning approaches can approach the accuracy of conventional methods, but direct evidence in complete-arch edentulous cases with a calibrated framework is limited and this study provides new comparative data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 years or older.
* Completely edentulous maxilla and mandible for at least 6 months following the last tooth extraction.
* Angle's Class I maxillomandibular relationship with adequate interarch space.
* Sufficient residual alveolar bone quantity and quality to receive dental implants.
* Good oral hygiene.
* Free from uncontrolled systemic diseases or conditions that may interfere with implant osseointegration.
* Able and willing to provide written informed consent.

Exclusion Criteria:

* Temporomandibular joint disorders or parafunctional habits.
* Heavy smokers.
* Uncontrolled systemic diseases.
* History of chemotherapy or radiotherapy to the head and neck region.
* Poor neuromuscular coordination.
* Localized bone defects that could compromise implant placement.

Where it's running

  • Noor Alhuda Rahemm Khalil
    Al Mansurah, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.