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Comparison of Accuracy of Full-arch Implant Digital and Conventional Impressions.

Comparison of the Accuracy of Digital and Conventional Impression in Edentulous Arch

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07190820
Enrollment
24
Registered
2025-09-24
Start date
2025-10-30
Completion date
2026-12-31
Last updated
2026-06-10

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

Conditions

Edentulous Jaw

Keywords

digital impression, implant restoration

Brief summary

The goal of this clinical trial is to determine whether the accuracy of digital impressions is comparable to conventional impressions. It will also learn about the clinical effect of different method. The main questions it aims to answer are: Does drug ABC lower the number of times participants need to use a rescue inhaler? What medical problems do participants have when taking drug ABC? Researchers will compare digital impression to conventional impression to see if the accuracy of the digital method. Participants will: Take an impression with one of the methods Visit the clinic a total of 6 times for checkups and tests

Interventions

complete arch implant impression with intraoral photogrammetry

conventional open tray splint impression

Sponsors

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Aged 30-80 years (inclusive) with no gender restriction. * Patients who will receive a full-arch one-piece implant-supported fixed * permanent restoration in the maxilla or mandible. * Patients with osseointegrated implants after surgery. * Patients voluntarily participate in the trial and sign the informed consent form.

Exclusion criteria

* Patients with insufficient interarch space in the posterior region for impression coping placement. * Patients with minimal inter-implant distance may prevent impression coping installation. * Patients with temporomandibular joint (TMJ) disorders are unable to maintain prolonged mouth opening for impression procedures. * Other conditions deemed ineligible for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Vision and tactile score for evaluating passive fit of metal frameworkPeriprocedural: At the time of the titanium framework try-in: the try-in of the framework to the patient is before final delivery. (The delivery of the final prosthesis is the baseline)Five aspects are evaluated, each aspect is scored as 0 or1. The score ranges from 0 to 5 points. 1、Framework rocking upon seating?2、 Gap assessment with single screw test. The method utilized an explorer with an approximately Ø60-µm tip to evaluate the margins of the metal framework.3、 Gap assessment with all screws tightened. 4、Are the screws threading smoothly? 5、Radiographic assessment of framework fit (check for gaps).

Countries

China

Outcome results

None listed

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